Recall events
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Event 93858
Event summary
Timeline bucket January 03, 2024
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording United Orthopedic Corporation
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
3 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 3
USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers: REF: PE11151211 - 11x150mm, PE11151213 - 13x150mm, PE11151215 - 15x150mm, PE11151217 - 17x150mm, PE11151411 - 11x200mm, PE11151413 - 13x200mm, PE11151415 - 15x200mm, PE11151417 - 17x200mm,
Z-1215-2024
Recall number Z-1215-2024
Initiated January 03, 2024
Classification Class II
Status Ongoing
Quantity 598 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential that the implant curved stem may be oriented incorrectly.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1215-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5210]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential that the implant curved stem may be oriented incorrectly.
Code information UDI(s): 04719872153894, 04719872153924, 04719872153863, 04719872153870, 04719872149866, 04719872153900, 04719872153917, 04719872153887 Lot Number(s): 15E198AA 15E198AA12 15E198AA22 15E198AA23 15E198S11 15E198S12 15E198W11 15E198W111 15E198X 15E198X21 15E198Y 15E198Y11 15E198Z 15E198Z111 15E198Z22 15E198Z3 16C168H 16C168H21 16C168H3 16C168J 16C168R1 17H618E 17H618E1 17H618E2 18A004A 18A004B 18A004B111 18A004C2 18A004C31 18A004D 18A004D1 18A004D21 18A004D22 18A004E 18A004E1 18A004E112 18A004F 18A004F111 18A004F211 18A004F212 18A004G 18A004G1 18A004G111 18A004G2 18A004G31 18A004H 18A004H212 18A004W11 20G378F2 20H134A 20H134A11 20H134A3 20H134B2 21D124A 21D124A1 21D124A2 21D124C1 21D124C11 21D512C 21D512C1 21D512C11 21D512D 21D512D2 21D512E2 21D512E3 21D512F1 21G420E1 21G420K1 21G420K11 21G420M1 21G420M2 21H573H1 21M254A 21M254B 21M254B1 21M254K 21M254X 21M254Y 21M254Y2 21M254Z 22F087AG 22F087AH 22F087AH1 22F087AJ 22F087AJ1 22K035C 22M166H 22M166J 22M166K 22M166K1 23A240C 23A240E 23A240E1 23A240F 23B622AA 23B622AB 23B622AC 23B622AD 23B622AW 23B622H 23B622J 23B622K 23B622L 23B622M 23B622N 23B622P 23B622Q 23B622R 23B622S 23B622W 23B622X 23B622Y 23B622Z 23C803W 23C803X 23D393L 23D393M 23D393N
Distribution pattern US: CA,KY, MI, IN, TN, CO, FL, TX, NV, OUS: Switzerland, United Kingdom, Malaysia, Philippines, Taiwan
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[36951]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 3
USTAR II Knee System Cemented curved stem, RHS, Non Coated for the following reference numbers: REF: PE25153109 - 9x125mm, PE25153209 - 9x150mm, PE25153113 - 13x125mm, PE25153111- 11x125mm, PE25153115 - 15x125mm, PE25153211 - 11x150mm, PE25153213 - 13x150mm, PE25153217 - 17x150mm, PE25153117 - 17x125mm, PE25153015 - 15x100mm, PE25153215 - 15x150mm
Z-1216-2024
Recall number Z-1216-2024
Initiated January 03, 2024
Classification Class II
Status Ongoing
Quantity 479 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential that the implant curved stem may be oriented incorrectly.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1216-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16878]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential that the implant curved stem may be oriented incorrectly.
Code information UDI(s): 04711605584562 04711605584579 04711605584586 04711605584616 04711605584630 04719872149866 04719872153542 04719872153559 04719872153566 04719872153573 04719872153610 04719872153658 04719872153665 04719872153672 04719872153689 04719872153696 04719872153863 04719872153870 04719872153887 04719872153894 04719872153900 04719872153917 04719872153924 04719872154341 04719872154358 04719872154365 04719872154372 04719872154389 04719872154396 04719872154402 04719872154419 Lot Number(s): 15E198AA 15E198S11 15E198Y 15E198Z 15E198Z111 16C168H 16C168H3 16C168J 16F306B2 16F306C 16F306C1 16F306E121 16H278K1 16H278K111 16H278K3 16H278L1 16H278L31 16H278N2 16H280D1 16H280D31 16H280D4 16H280E1 16H280E11 16H280E3 16H280F11 17B448AY13 17H618E1 18A004B 18A004C2 18A004D 18A004D1 18A004F 18A004G 18A004G1 18A004W11 18C255FG 18C255FG11 18C255FG12 18C255K31 18C255R 18C255W11 18C255X 18C255X1 18C255Y131 18C256A122 19G738DN 19G738DN12 19G738DN3 19G738DP 19G738DQ 19G738DR12 19G738DW12 19K248AR 19K248AS 19L428CZ2 19L428W2 19L496C 19L496C1 19L496C111 19L496D 20B320X 20B320X11 20E324AC12 20E324AK 20E324AK1 20E324AK2 20E324AL 20E324AM 20E324AM11 20E324AN 20E324B 20E324B11 20E324C 20E324C11 20E324D 20E324D1 20E324Q 20E324Z121 20E325AP 20E325AP11 20E325CD 20E325CE11 20E325CE2 20K450AM2 20K450AM21 21A648C 21A648C21 21A648R2 21A648S11 21A648S111 21D124A 21D512D 21F303N 21F303P 21F303P11 21F670C11 21F670D11 21F670D2 21F670D21 21F670D3 21G420M1 21G420M2 21H573H1 21K409N1 21K409P2 21K409Q2 21M254Y 21M750BF 21M750BG 21M750BH 21M750BJ 21M750BJ1 21M750BK 21M750CG 21M750CG1 22A822D 22B220AE 22B220AE1 22B220AF1 22J283BS 22J283BS1 22J283BS2 22J283CR 22M655AQ 23B622AW 23B622L 23B622M 23H820H
Distribution pattern US: CA,KY, MI, IN, TN, CO, FL, TX, NV, OUS: Switzerland, United Kingdom, Malaysia, Philippines, Taiwan
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[36348]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 3
USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: PE25153109 - PE25151109 - 9x125mm, PE25151111 - 11X125, PE25151113 - 13X125mm, PE25151115 - 15X125mm, PE25151117 - 17X125mm, PE25151119 - 19X125mm, PE25151209 - 9X150mm, PE25151211 - 11X150, PE25151213 - 13X150mm, PE25151215 - 15X150mm, PE25151217 - 17X150mm, PE25151415 - 15x200mm
Z-1217-2024
Recall number Z-1217-2024
Initiated January 03, 2024
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential that the implant curved stem may be oriented incorrectly.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1217-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16882]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential that the implant curved stem may be oriented incorrectly.
Code information UDI(s): 04711605584562 04711605584579 04711605584586 04711605584616 04711605584630 04719872149866 04719872153542 04719872153559 04719872153566 04719872153573 04719872153610 04719872153658 04719872153665 04719872153672 04719872153689 04719872153696 04719872153863 04719872153870 04719872153887 04719872153894 04719872153900 04719872153917 04719872153924 04719872154341 04719872154358 04719872154365 04719872154372 04719872154389 04719872154396 04719872154402 04719872154419 Lot Number(s): 15E198AA 15E198S11 15E198Y 15E198Z 15E198Z111 16C168H 16C168H3 16C168J 16F306B2 16F306C 16F306C1 16F306E121 16H278K1 16H278K111 16H278K3 16H278L1 16H278L31 16H278N2 16H280D1 16H280D31 16H280D4 16H280E1 16H280E11 16H280E3 16H280F11 17B448AY13 17H618E1 18A004B 18A004C2 18A004D 18A004D1 18A004F 18A004G 18A004G1 18A004W11 18C255FG 18C255FG11 18C255FG12 18C255K31 18C255R 18C255W11 18C255X 18C255X1 18C255Y131 18C256A122 19G738DN 19G738DN12 19G738DN3 19G738DP 19G738DQ 19G738DR12 19G738DW12 19K248AR 19K248AS 19L428CZ2 19L428W2 19L496C 19L496C1 19L496C111 19L496D 20B320X 20B320X11 20E324AC12 20E324AK 20E324AK1 20E324AK2 20E324AL 20E324AM 20E324AM11 20E324AN 20E324B 20E324B11 20E324C 20E324C11 20E324D 20E324D1 20E324Q 20E324Z121 20E325AP 20E325AP11 20E325CD 20E325CE11 20E325CE2 20K450AM2 20K450AM21 21A648C 21A648C21 21A648R2 21A648S11 21A648S111 21D124A 21D512D 21F303N 21F303P 21F303P11 21F670C11 21F670D11 21F670D2 21F670D21 21F670D3 21G420M1 21G420M2 21H573H1 21K409N1 21K409P2 21K409Q2 21M254Y 21M750BF 21M750BG 21M750BH 21M750BJ 21M750BJ1 21M750BK 21M750CG 21M750CG1 22A822D 22B220AE 22B220AE1 22B220AF1 22J283BS 22J283BS1 22J283BS2 22J283CR 22M655AQ 23B622AW 23B622L 23B622M 23H820H
Distribution pattern US: CA,KY, MI, IN, TN, CO, FL, TX, NV, OUS: Switzerland, United Kingdom, Malaysia, Philippines, Taiwan
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[37146]
FDA event record
· Exact recall-number query on openFDA
