Recall events
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Event 93595
Event summary
Timeline bucket December 05, 2023
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording Oakworks 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
4 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 4
Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An Ultrasound examination table
Z-0727-2024
Recall number Z-0727-2024
Initiated December 05, 2023
Classification Class II
Status Ongoing
Quantity 212 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Backrest platform stress fracture - the table is not operational in an inclined position
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0727-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[40615]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Backrest platform stress fracture - the table is not operational in an inclined position
Code information (UDI): 00817463025323 S/N: Serial Number USE837298 USE837299 USE832277 USE832279 USE812943 USE814317 USE799725 USE799726 USE799727 USE799730 USE799732 USE802575 USE802576 USE811024 USE811257 USE811258 USE811259 USE811260 USE811261 USE812704 USE813219 USE813603 USE818072 USE819626 USE824702 USE825956 USE825957 USE825958 USE825959 USE825960 USE826294 USE829080 USE829705 USE829706 USE829707 USE829708 USE829709 USE829710 USE832003 USE832004 USE832005 USE832006 USE832007 USE834846 USE835241 USE835242 USE835476 USE835776 USE836792 USE836879 USE836880 USE836881 USE836882 USE813594 USE813595 USE817820 USE839073 USE839074 USE839075 USE839076 USE814826 USE814827 USE814828 USE814829 USE814830 USE827308 USE803256 USE803299 USE803300 USE805960 USE805961 USE805962 USE809599 USE812579 USE815868 USE815908 USE817060 USE817061 USE818707 USE822030 USE824612 USE826254 USE828213 USE828214 USE829403 USE832116 USE832990 USE833712 USE833713 USE833960 USE838977 USE838254 USE805081 USE805082 USE818815 USE806583 USE811236 USE818243 USE819259 USE825037 USE835200 USE818139 USE818140 USE835527 USE835528 USE809360 USE811590 USE801767 USE805493 USE805494 USE805495 USE805794 USE805795 USE806093 USE806343 USE806782 USE806783 USE806784 USE807732 USE807827 USE807828 USE807832 USE807833 USE807834 USE807835 USE807836 USE807837 USE808960 USE808961 USE808962 USE809182 USE809631 USE809632 USE810336 USE810546 USE813715 USE813912 USE813913 USE813914 USE814416 USE814417 USE814418 USE816892 USE817024 USE817174 USE817457 USE817675 USE819750 USE822988 USE822989 USE823802 USE831280 USE831313 USE832776 USE834440 USE834875 USE834876 USE835877 USE836209 USE838838 USE838920 USE813405 USE805279 USE805280 USE805281 USE809749 USE809750 USE809751 USE809752 USE812563 USE812564 USE812565 USE812566 USE814568 USE817617 USE820048 USE833660 USE834269 USE835798 USE835799 USE835800 USE835801 USE835802 USE835803 USE835804 USE830284 USE811539 USE812084 USE816038 USE803752 USE801427 USE803589 USE839292 USE813104 USE813719 USE810378 USE810379 USE835126 USE838175 USE817021 USE839597 USE839598 USE818132 USE818133 USE818134 USE818135 USE818136 USE818137 USE818138 USE802125 USE826701 USE831873
Distribution pattern US Nationwide Distribution
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[37103]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 4
Ultrasound EA (Ergonomic Advantage) table versions; G3 (General 3 Section) Echocardiography -An Ultrasound examination table
Z-0728-2024
Recall number Z-0728-2024
Initiated December 05, 2023
Classification Class II
Status Ongoing
Quantity 104 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Backrest platform stress fracture - the table is not operational in an inclined position
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0728-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5144]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Backrest platform stress fracture - the table is not operational in an inclined position
Code information (UDI): , 00817463025439 S/N: USW821950 USW821951 USM838906 USM838908 USM838909 USM838910 USM838911 USM838912 USW833604 USW803220 USW810646 USM802363 USM802364 USM802365 USM802366 USM802367 USM802368 USM802369 USM802370 USM802371 USM802372 USM802373 USM806418 USM806419 USM824495 USW824575 USW824576 USW835742 USW835743 USW835744 USW835745 USW835870 USW835871 USW805335 USW805500 USW814481 USW814489 USW814490 USW814491 USM818829 USM818830 USW834435 USW834436 USW834437 USW834438 USW837136 USW837137 USW837138 USW837139 USW837140 USM834172 USW825108 USW836285 USW825254 USW825255 USW825256 USM832158 USM837032 USM805639 USM805640 USW809784 USW809785 USW810360 USM810619 USW811819 USW825625 USW825626 USW833747 USW806381 USW809243 USW810505 USM814053 USM814054 USM814055 USW829084 USW838113 USW838114 USW807763 USW800305 USM812019 USM812024 USM820560 USW832338 USM827491 USM805539 USM813172 USM813173 USM806277 USW817676 USW817677 USW818075 USW829140 USM809220 USM809200 USM809202 USM797137 USM819374 USM819375 USM819376 USM819377 USM819378 USM819379 USM819381 USM819382
Distribution pattern US Nationwide Distribution
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[33834]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 4
Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography and Multi-Specialty with Electric Access Back Supports [left & right}
Z-0729-2024
Recall number Z-0729-2024
Initiated December 05, 2023
Classification Class II
Status Ongoing
Quantity 20 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Backrest platform stress fracture - the table is not operational in an inclined position
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0729-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46392]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Backrest platform stress fracture - the table is not operational in an inclined position
Code information (UDI): 00817463025422 S/N: USM839457 USM839458 USM839459 USM839460 USM839461 USM818212 USM833897 USW813999 USM839614 USM839615 USM814871 USM833507 USM831797 USM823858 USM822620 USM824500 USM834529 USM788091 USM815794 USM832170
Distribution pattern US Nationwide Distribution
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[36998]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 4
Ultrasound EA (Ergonomic Advantage) table version; V2 (Vascular 2 Section) Echocardiography -An Ultrasound examination table
Z-0730-2024
Recall number Z-0730-2024
Initiated December 05, 2023
Classification Class II
Status Ongoing
Quantity 28 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Backrest platform stress fracture - the table is not operational in an inclined position
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0730-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5143]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Backrest platform stress fracture - the table is not operational in an inclined position
Code information (UDI): 00817463025521 S/N: VCF805597 VCF814488 VCF814750 VCF817222 VCF817223 VCF817720 VCF817721 VCF823450 VCF825629 VCF825630 VCF833350 VCF813968 VCF817520 VCF826533 VCF822117 VCF824501 VCF824502 VCF824503 VCF824504 VCF815120 VCF814849 VCF835728
Distribution pattern US Nationwide Distribution
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[36814]
FDA event record
· Exact recall-number query on openFDA
