1) Accolade II 127 Neck Angle Hip Stem — Class II medical device recall Z-0467-2014
Terminated recall by Stryker Howmedica Osteonics Corp., reported 2013-12-18, distributed nationwide. Stryker received a report from the field indicating that an Accolade II Hip Stem Size #3 was identified in pac
| Recall number | Z-0467-2014 |
|---|---|
| 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 | 2013-10-25 |
| Classified | 2013-12-07 |
| Reported by FDA | 2013-12-18 |
| Terminated | 2015-03-31 |
| Distributed | Nationwide (US) |
| Quantity | 20 units |
| Lot numbers | 44416307, 44564405 |
| Model numbers | 6721-0330, 6721-0535 |
Product
1) Accolade II 127 Neck Angle Hip Stem, Size # 3 2) Accolade II 127 Neck Angle Hip Stem, Size #5 Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA Telephone # +1 201-831-5000 Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 MEYZIEU Cedex France Intended for cementless application in total or hemiarthroplasty procedures.
Reason for recall
Stryker received a report from the field indicating that an Accolade II Hip Stem Size #3 was identified in packaging with an Accolade II Hip Stem Size #5.
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-0467-2014. 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.