Special Orthopaedic Solution Peri-Acetabular Prosthesis V40 Femoral… — Class II medical device recall Z-0286-2013
Terminated recall by Stryker Howmedica Osteonics Corp., reported 2012-11-21, distributed nationwide. Stryker has become aware that insufficient taper torsional strength may result when a PAR extension piece is u
| Recall number | Z-0286-2013 |
|---|---|
| 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 | 2012-07-16 |
| Classified | 2012-11-13 |
| Reported by FDA | 2012-11-21 |
| Terminated | 2015-09-09 |
| Distributed | Nationwide (US) |
| Quantity | 301 units |
| Reason classes | potency |
Product
Special Orthopaedic Solution Peri-Acetabular Prosthesis V40 Femoral Extension Component Product Usage: The PAR extension piece is a component of the PAR assembly. The Peri-Acetabular Reconstruction (PAR) endoprosthesis was developed to meet the unique needs of patients who require reconstruction of large acetabular defects after a Type I and II pelvic resection.
Reason for recall
Stryker has become aware that insufficient taper torsional strength may result when a PAR extension piece is used with a forged CoCr stem.
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-0286-2013. 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.