Stryker Orthopaedics Universal Acetabular Cup Positioner/Impactor — Class II medical device recall Z-0060-2017
Terminated recall by Stryker Howmedica Osteonics Corp., reported 2016-10-19. Stryker Orthopaedics has received reports of the thread length protruding past the dome of the acetabular tria
| Recall number | Z-0060-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Howmedica Osteonics Corp., Mahwah, NJ, United States |
| Recall initiated | 2016-08-18 |
| Classified | 2016-10-07 |
| Reported by FDA | 2016-10-19 |
| Terminated | 2018-08-01 |
| Quantity | 3,768 units |
| Lot numbers | SAMPLE25, SMM09N05, SMM09N08, SMM09V06, SMM0M02, SMM0T00A, SMM0T00K, SMM6C00, SMM6N00, SMM6N01, SMM6N01A, SMM6N02, SMM6N03, SMM6N04, SMM6N04A, SMM7A00, SMM7A00E, SMM7A00L, SMM7A01T, SMM7A01TD, SMM7A01TDD, SMM7A01TT, SMM7A02, SMM7A02A, SMM7A02E, SMM7A02EE, SMM7A02T, SMM7C01, SMM7C01T, SMM7C01TT, SMM7C01TW, SMM7C01W, SMM7C02, SMM7C02H, SMM7C02J, SMM7E00, SMM7E01, SMM7E01A, SMM7E01JK, SMM7E01T and 321 more |
| Model numbers | 2101-0200 |
Product
Stryker Orthopaedics Universal Acetabular Cup Positioner/Impactor, REF 2101-0200, Non-Sterile, Howmedica Osteonics Corp., Mahwah, NJ, USA, A Subsidiary of Stryker Corp.
Reason for recall
Stryker Orthopaedics has received reports of the thread length protruding past the dome of the acetabular trial or implant for the Trident Universal Impactor/Positioner.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0060-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.