Recall events
/
Event 83594
Event summary
Timeline bucket August 15, 2019
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Zimmer Biomet, Inc.
Dossier provenance
Source snapshots represented here
openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Complete imported group
Every recalled product in this event
35 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 35
XP- CR Tibial Tray- Interlok 59mm Item # 195268
Z-2503-2019
Recall number Z-2503-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 45 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2503-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11205]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 004960 262370 130580 004970 130630 130550 130610 130560 130570 004950 130590 279210
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8717]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 35
XP-CR Tibial Tray - Interlok 63mm Item # 195269
Z-2504-2019
Recall number Z-2504-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 322 unit
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2504-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32846]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 663420 993820 660430 660430R 262380 395340 445350 584240 562230 578990 579070 043840 159200 917670 996050 043840R 917670R 206800 090150 159210 352790 995940 352780 469480 321920 663450 258040 352770 966700 434250 434260 456730 274630 374760 672430 899750 041270 899710 041200 666860 278990 600750 712530 600750R 821250 821250R 450310 599050 599050R 199780 717140 943340 017920 076390 220020 220020R 175270 228580 175270R 199790 199790R 395350
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[12230]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 35
XP-CR Tibial Tray - Interlok 65mm Item # 195270
Z-2505-2019
Recall number Z-2505-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 375 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2505-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[22393]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 666880 660440 579080 579170 993790 262390 228590 584250 289150 579150 663480 996060 663480R 043850 090170 917690 159220 321940 352810 374770 600760 663500 841510 076020 352800 383660 429220 966710 321970 456740 456740R 995950 258050 274610 274600 403820 206810 041210 899720 899760 585520 585520R 041280 503430 437500 503490 503420 247240 247240R 374010 712540 672470 279000 575960 017940 450320 599100 717150 599100R 943350 821270 111560 220030 175280 199800 199810 175280R 395360 395370 395390 445360 395390R
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[9878]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 35
XP-CR Tibial Tray - Interlok 67mm Item # 195271
Z-2506-2019
Recall number Z-2506-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 567 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2506-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[50401]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 486100 262400 291180 584260 663550 562250 666830 660450 841520 917700 966720 966720R 075450 075460 075500 663530 995960 322020 043860 090190 206820 075440 745670 352820 383680 075470 745650 513340 159230 258060 429230 161960 161950 161930 161910 161920 162010 161860 274480 161870 161900 274460 996070 274490 274510 721690 322000 456750 456750R 274470 374780 951150 075510 469490 721670 309710 274500 309680 309690 075490 309700 585540 883560 221140 374030 920540 279010 450330 672510 575980 821280 943360 599120 600770 712550 717160 017970 076400 076410 220040 175290 175290R 289160 676270 676300 228610 351290 395400 395420 445370 395400R
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8734]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 35
XP-CR Tibial Tray - Interlok 69mm Item # 195272
Z-2507-2019
Recall number Z-2507-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 498 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2507-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32851]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 562270 579210 663600 262410 445380 584280 590680 660460 663580 190400 190450 190460 190480 190470 190440 190490 190420 663620 996080 663620R 579230 043870 043880 090200 159240 090200R 159250 258070 283160 995970 206830 966730 374790 383690 283150 283150R 590690 352830 429250 322040 469500 456760 041290 827550 827540 585560 041220 503500 076030 221160 374060 221150 279020 712560 576010 672540 374050 821300 943380 450340 599130 600780 717170 017990 111580 111570 821290 220050 289180 121130 202930 218640 199730 351300 395430 395450 439670 445390 486110 351300R 395450R 439670R
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8672]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 35
XP-CR Tibial Tray - Interlok 71mm Item # 195273
Z-2508-2019
Recall number Z-2508-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 454 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2508-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44589]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 663640 262420 571030 590700 590710 676280 917650 320580 966740 995980 996090 966740R 043890 159270 206840 258080 283210 841530 043900 066200 090220 066200R 322070 322070R 383700 352840 283180 359640 322090 429260 374800 403830 159260 456770 041150 579240 899740 274590 274530 274580 041240 041190 503440 585580 993810 666890 503460 888430 221170 985320 374080 374070 279030 599140 576020 943390 821310 411240 450350 600790 712570 717180 717180R 018020 111590 676310 676310R 072520 218650 291200 072520R 672570 289190 562280 148430 291190 351320 445400 445410 486120 445400R 445410R
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8686]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 35
XP-CR Tibial Tray - Interlok 73mm Item # 195274
Z-2509-2019
Recall number Z-2509-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 327 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2509-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44594]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 553880 590760 663690 553880R 590750 663670 262430 513080 663720 513080R 472990 938180 578980 090230 159280 676320 258090 043920 066220 206850 322110 352860 841550 917740 966760 283230 374810 283240 996010 352850 352850R 429270 851300 383710 041300 585600 076010 469520 578970 599150 600800 600800R 279040 450360 672600 374090 943410 712580 121150 018040 821330 121140 199740 218670 717190 308100 308110 502840 513070 571040 502840R 513070R 571040R
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[9949]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 35
XP-CR Tibial Tray - Interlok 75mm Item # 195275
Z-2510-2019
Recall number Z-2510-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 369 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2510-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57250]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 663790 262440 513090 590770 590780 590790 663740 663770 917760 206860 938190 966780 206860R 043930 066230 090240 851340 322130 258100 283250 434280 434280R 429280 456780 513110 434270 996020 374820 469540 041250 666900 041160 579270 503470 503450 503410 576030 279050 599160 672640 374100 821350 821350R 450370 600810 712590 717200 600810R 717200R 148450 199750 676260 676330 676290 562300 562300R 279260 308120 308130 473000 502860 553890 571050 279260R 308120R 473000R
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8747]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 35
XP-CR Tibial Tray - Interlok 79 mm Item # 195276
Z-2511-2019
Recall number Z-2511-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 319 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2511-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11204]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 663820 503480 262450 308140 308150 473010 513130 320340 320590 579060 571060 938200 322150 066240 283270 322200 851360 996030 996030R 090250 841560 206870 322180 258110 279270 553900 711510 161980 161990 274450 043940 041260 663840 041170 993800 883570 883600 883590 883580 888420 374120 599170 576060 279060 712600 576050 672660 821370 600820 717210 943420 221180 141500 199770 450380 220060 502880 513120
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[12228]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2512-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 180 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2512-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[50400]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 141540 513160 571080 262460 938230 938260 966800 996040 066250 283280 663860 851390 663860R 090260 279290 376610 851380 663890 206880 374840 429310 723100 434300 469560 469560R 162000 258130 043950 320350 320330 076100 279070 600830 672690 599180 374130 576070 952400 450390 712610 717220 943430 141520 279280 376570 376590 513140
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[12502]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2513-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 78 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2513-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[22392]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 966230 262470 587200 274370 274360 274380 274420 715690 274420R 715690R 393650 279080 394490 821380 903430 943440 422480 512580
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8728]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2514-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 82 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2514-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27851]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 262480 960510 274400 274430 336060 336060R 274390 274410 279280 394540 394590 394570 821400 903420 960530 422490 512590
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8726]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2515-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 2 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2515-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32852]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Numbers 149710 615950
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8754]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2516-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 86 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2516-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[50394]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 183700 790980 202030 202020 202010 986220 986240 986240R 396520 986230 394870 394840 833310 394860 903470 508690 701050 701050R
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[9861]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2517-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 90 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2517-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[38656]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 790970 984810 984820 202000R 664250R 664280R 685040 885800 716010 873630 903460 960480 960500 201990 202000 664250 664280 400690 394670 394710 293220 183680 394330
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8679]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2518-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 384 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2518-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3477]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 559070 527660 677630 191210 219890 677620 758460 089950 283100 358850 283080 374620 321750 321770 358830 374580 374590 420310 420320 434060 358860 381760 321690 358840 468200 381770 381780 381780R 321710 434070 420290 468210 023420 011510 864760 093450 093460 885140 855480 975650 828760 061480 331670 103080 131270 159350 116110 223220 116110R 587400 181490 418770 634280 664240 783170 716000 906810 685020 882160 882170 881950 715990 986210 396500 986200 906820 029310 126100 163080 247440 293200 293210 163090 126090 920640 920640R 481960 073030 374570 442040 442050 318630 479060 509960 509930 450480 183670 479050 576240 543440 543450 625770 593670 639750 670660 758590 741610 481970 943600 808440 917680 951040 780300 833290 851020 873620 481950 018270 999420 076780
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8744]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2519-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2519-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27850]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 664420 664430 677600 677610 219880 841630 158920 158940 758430 758450 102010 972850 998140 089940 998150 101990 101980 273110 972840 036320 283060 322560 273120 273120R 322570 592590 592600 592550 703470 703530 703480 703540 703580 592560 703450 703490 703510 703570 703590 703500 703520 592610 703550 283040 592580 703460 790990 102000 592570 703600 791020 828750 703610 966270 061470 093430 703620 975640 011500 023410 061460 093440 703560 855460 864750 131260 116090 103070 241490 181480 201980 223200 159340 885130 336760 090000 297100 371660 467260 418760 371670 432440 556610 261120 585790 384310 511500 587390 634320 530660 384300 664230 685000 715980 882150 715960 906780 906800 920630 715970 126070 126080 073010 029300 396490 986060 163050 986090 221460 247420 163070 247410 293180 293190 318620 374550 374560 318600 442030 390200 390220 442020 478600 509910 543420 576220 576230 450470 479020 509880 543430 593660 625720 625740 639730 670640 560390 708800 741590 741600 708810 183560 481920 481930 481940 780270 851000 481910 559060 758580 780290 999410 808410 833270 873610 917670 943590 999400 111760 076760 018260 076770 851010 137540 111740 018220 261930 191200 261950 289270
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8863]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2520-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 973 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2520-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44588]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 664400 664380 677580 562210 758380 650470 677760 677590 677750 758410 664390 664410 677570 613450 972810 972820 998120 158870 677770 677780 998110 283010 273090 273100 677740 703240 592490 592490R 592530 592620 703080 592660 703160 703160R 558590 592640 592650 592640R 558580 703090 703120 282950 505130 505140 703100 703190 703230 703260 703200 158890 283020 558570 592510 592520 592630 677720 703070 703170 703210 791010 592520R 322550 322530 592500 885120 975630 505160 864740 958470 855430 592540 703150 828740 505150 703060 703130 703140 703060R 840750 103060 131250 159330 131250R 011490 061450 093420 181470 703180 023400 116070 201970 036310 336740 241480 223190 261110 297090 371620 371640 384280 418750 432410 634300 599880 556600 664220 467240 511490 715900 715910 587370 684980 716120 920620 882120 906770 029290 906760 986000 072990 986030 396430 126060 163040 163060 247400 247390 705700 126050 293160 318590 293170 374530 336750 336760 374540 390140 442010 390170 442000 318580 478980 479000 479010 509860 509840 576200 543410 576210 625670 639710 625690 543400 450460 741570 780260 758570 780280 522710 559050 221440 670630 741580 708770 593650 481900 833240 873590 183550 808360 873580 850980 850990 808390 708780 076750 999390 560380 570300 570310 111730 076730 917660 951010 076740 943570 018190 137530 999380 191190 219870 289250
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[7546]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2521-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 906 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2521-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3478]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 562200 664340 613420 512640 820800 820820 650460 422530 820780 677550 589910 664350 664360 664370 677540 677560 972780 758360 758340 972800 089920 101940 158830 273080 158830R 101950 158840 207050 101960 036290 036300 322490 998100 282810 322510 358980 434000 434000R 282840 434050 101970 207040 358990 468160 499260 505110 468170 505120 499270 499270R 558560 558540 273050 505100 558550 282880 207030 434010 499280 864730 885110 592460 916870 791000 916880 592480 828730 885100 434040 592470 505090 840740 061430 061440 499290 975620 093410 958450 011480 103050 159320 223170 261100 293920 293890 293910 297080 131240 181450 181460 201960 241470 855400 337030 336160 371610 384240 998090 371600 116050 432340 592450 023390 336150 384260 511480 418740 599840 556590 634270 467220 664210 716110 684960 705680 715890 587340 920610 985960 882110 906750 906740 985980 029280 072950 072970 126030 126040 163020 221420 396410 163030 247370 247380 293140 293150 318560 318570 336740 374510 374520 390120 441990 336730 390100 441970 441980 478970 478950 509820 533610 450450 509790 576180 625640 639690 543380 593640 543390 625610 481890 576190 670610 708700 741550 741560 559040 560370 808330 183530 306440 808320 570290 850970 873570 833210 850960 873560 758550 780250 758560 780240 999370 943550 950990 018170 917650 999350 999480 522680 570280 137520 219830 111720 191180 076710 076720
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[11233]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2522-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 1221 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2522-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[38658]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 450440 590880 512630 820720 820750 841600 841620 664320 841610 972770 589900 660500 664300 664310 677650 841580 664300R 972750 998070 758320 044000 841590 044020 066160 677640 066150 381750 420270 664330 381750R 381730 433990 374560 282790 374540 420280 433960 381740 358960 758290 468150 505080 036280 998080 089890 358970 374570 499170 505060 358970R 374570R 322450 282800 499150 420250 499160 499180 592370 468140 505070 592380 592350 322460 036270 505050 840730 885090 840710 855340 864720 885080 592360 592400 916860 958440 916850 828720 975610 958430 011470 023380 061400 061410 984770 181440 103040 181420 103030 131230 159310 061420 116010 116030 261080 293870 241450 297200 336140 293850 223150 241440 261090 384230 336980 337000 093400 223130 201950 297070 371590 336130 556580 587300 371560 418730 432380 384220 467200 511470 599810 599810R 634230 664180 684930 705650 715820 716100 715830 715840 715840R 882100 920600 906730 906720 029270 072940 985950 072920 126020 985940 396390 126010 163000 163010 247340 247360 247350 221400 293130 318540 293120 318530 336720 318510 336710 374470 374490 390050 318520 390070 570260 478910 478920 478940 441940 441950 441960 509740 543370 543350 509780 593630 625550 522640 576160 576170 593620 625570 639660 639670 670580 708620 670590 708540 741540 780230 758540 808280 522660 560360 780210 808300 570270 741530 758530 850950 850940 833190 873550 873540 917630 999330 999340 018150 999470 076700 111700 917640 943540 950970 999460 076690 111710 183520 481870 481880 559030 481880R 072650 137510 191160 219820 289240 562190 613400 650440 650450 422520
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[9869]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2523-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 1282 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2523-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[38660]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 590860 660490 590850 560350 562180 650420 758270 841570 650430 613370 303400 589890 972740 998060 998040 972730 043990 066130 101900 174980 282760 101920 174970 207000 258020 101920R 066140 101890 101930 258030 036260 322420 374530 374550 358950 358950R 036250 358940 207020 336660 207010 420360 336960 558600 558610 592310 374520 420400 592340 282770 592330 499140 499130 499130R 381700 381710 499110 322400 381720 802050 855300 802050R 802060 840700 864710 802060R 061380 223100 885070 958400 975590 975600 011450 023370 958410 984760 011440 499120 828710 166070 885060 916840 916840R 840690 558620 061390 115970 131220 115990 159300 181400 093390 181410 201940 103020 293790 223090 297190 293820 592290 418710 336120 418700 336100 418690 420380 467190 599780 511460 556570 634200 664170 705610 684910 587280 684900 297180 716090 705630 716080 715810 715790 882080 715800 715780 985910 985920 029250 906690 906710 029260 920580 072870 072890 125990 126000 162970 396350 432530 162990 221390 247330 293100 247310 247320 293110 318470 336700 318480 318500 336690 882090 389990 390020 374450 441910 478860 374420 441920 441930 478880 478890 509710 509720 543330 522630 543300 576140 576150 593600 593610 639640 639650 625500 625480 670550 450430 758520 708440 741510 570250 670560 758510 780190 833180 708470 741520 808230 808250 850930 780200 850920 873520 917620 943530 950960 873530 076670 076680 999320 183440 481860 522650 559020 570230 999440 999310 018130 999450 202940 303390 111690 219790 137500 111660 191140 512610 422510 590870
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[7550]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2524-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 1210 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2524-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32849]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 562170 613350 677700 677680 664240 758250 758230 753770 753780 998030 753790 590830 590840 660470 660480 664230 664260 664270 677660 677670 677710 590830R 677660R 677670R 972690 758210 972710 206980 174950 174950R 174960 206970 258000 258010 664290 664290R 664280 206960 282720 322360 468220 036240 219760 336620 359230 358920 592270 336640 592260 592260R 592230 592240 592250 592220 282740 322380 468230 358930 864700 802030 885040 802030R 802020 828700 828700R 975580 958380 840680 855270 011430 023360 061360 592200 916830 131190 093380 201930 223080 241430 103010 181390 159290 984750 297170 115960 261150 293750 958370 261160 336090 418680 432510 061340 587260 511450 599740 705580 634170 705560 664160 684880 715770 715750 716070 715760 716050 882070 985900 029240 906680 920570 029230 125980 396320 221370 072850 162930 162950 247270 247300 293090 318450 318460 336680 374390 374410 389960 441900 478840 478850 441890 298480 467170 509670 543250 543280 509690 576120 576110 593580 625460 639630 670540 708420 570220 741490 758500 570210 741500 780180 450420 522610 450420R 808210 833170 850900 850910 873500 873510 943520 999300 917610 950930 999430 183390 559010 560320 018100 111650 076660 191120 137490 422500 512600 650400 650410 571160 589780
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8692]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2525-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 857 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2525-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27852]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 590800 309530 579280 309460 590810 590820 309510 650390 562160 613330 758190 571150 589750 972670 029010 065310 029010R 206950 043980 065640 174940 043980R 174930 206930 257980 336590 206940 257990 028990 029000 783130 783160 801980 801980R 783100 885030 916820 864690 958350 958350R 783120 783150 855240 958340 840660 801970 023350 783080 036230 975570 984720 984740 011420 103000 159280 093370 061330 115950 131180 181380 297160 309500 511440 599700 467150 634140 664150 684850 664150R 587250 309480 705540 328040 715740 716040 241420 261140 882060 920560 029220 072830 906660 985890 396310 125970 162900 162920 221350 076130 247260 318440 374340 336670 374370 293080 441880 478800 478820 509650 509620 076090 543210 543230 576090 559000 559000R 576100 593570 450410 522600 639610 670520 708400 741480 741470 758490 780170 833160 183380 808180 850890 917600 873480 873490 963440 999290 999290R 943500 560300 570190 570200 018080 076650 137480 111640 191100 579300 219730 289200 261920
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[7566]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2526-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 480 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2526-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44595]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 522520 571140 589700 758150 028960 028980 043970 028980R 043970R 064960 028970 065200 101860 101880 065200R 433940 321620 321640 321620R 321640R 433910 592120 592140 592150 592170 257970 592180 801960 282710 282710R 282690 801940 801950 783060 783040 011410 975550 592110 984660 023340 257960 840190 061310 592160 102990 223050 261130 336080 585400 585370 511430 467140 684820 664140 634080 705510 715730 716030 716030R 920550 881940 029210 906640 985880 072790 125870 162880 396240 318430 247250 336660 441870 374320 587220 509590 543180 543150 708390 576080 639600 670510 522580 558990 593560 450400 741460 758480 780160 808130 833150 873470 943480 850880 917590 183370 560280 570170 570180 570180R 076640 191080 111620 950910 963430 999270 018060 261910 613310 650370
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[12473]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2527-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 50 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2527-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[15318]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 206540 057180 206590 206580 206550 030800 206560 457940 457880 457930 457970 457950
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[7564]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2528-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 8 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2528-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[15316]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 833140 332580 514890 764300 754440 837720 999580 999590 999570 764290 999610 090060 090020
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[9971]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2529-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 43 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2529-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44592]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 833150 332620 514900 752000 372950 752010 919200 837730 764310 764320 884350 883500 968960 968970 968980 754450 883450 584190 861150 660380
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[12490]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2530-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 74 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2530-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27853]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 332640 833160 514940 372960 372970 514920 752020 752030 919210 764330 754460 884550 837740 764340 861170 884360 887950 935780 935800 953910 968990 953950 928850 936190 953930 953940 861160 663120 660390 663080 663110 584200
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8706]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2531-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 123 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2531-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57251]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 117720 332660 373010 373000 514970 515000 372990 039210 112980 113000 112990 202920 303370 303380 590480 660400 660410 584210 590490 833180 752040 752050 752560 752060 919220 928860 754470 764360 837750 764350 846490 861180 881480 881490 928870 846500 881460 984370 984380 984360 837760 570940
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[12485]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2532-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2532-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[15314]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 584220 590500 590510 663160 663180 663170 660420 117730 332670 833200 373020 373040 373030 515030 515020 515040 752090 752070 752080 919240 919230 846510 764370 764380 837780 754480 837770 861200 881500 881510 984430 984400 039230 052240 039240 881530 984390 039220 984420 052260 984410 090340 570960
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[11222]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2533-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 84 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2533-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11201]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 590540 590530 590520 663190 590550 663200 907710 117740 332690 833210 752580 373050 373060 515050 752120 515070 752100 752110 754490 764390 861210 837790 936210 764400 846520 928890 907690 936220 936230 954050 928880 936200 954030 907700 063000 062990 570980 584230
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[9964]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2534-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 110 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2534-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[22389]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 833220 919250 919260 936260 764410 764420 837800 936240 846540 861190 928760 936250 954020 846530 928770 953990 928800 954000 928790 590580 571000 663280 590570 663250 663260 663270 590590 663240 663300 590560 332710 515110 373070 373080 515090 752140 752130 332740 754500
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[12511]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2535-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 99 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2535-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[22394]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 332750 833230 515120 752550 515130 373090 919280 754510 764430 764440 861230 837810 846560 907730 928810 907720 907740 969000 969010 590620 590600 663320 663330 663340 590610 571010 663310
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[11230]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2536-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity 49 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2536-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57253]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information Lot Number 332760 752520 515140 754520 063070 072460 072440 072510 663350 663360 833240 919270 764460 846570 764450 837820 861240 915690 915700
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[12217]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2537-2019
Initiated August 15, 2019
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The locking bar not fully engaging
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Manufacturing material removal
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2537-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44593]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The locking bar not fully engaging
Code information None distributed
Distribution pattern State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8811]
FDA event record
· Exact recall-number query on openFDA
