Accolade TMZF Plus 127 degree Neck Angle V40 Hip Stem #2 — Class II medical device recall Z-0656-2013
Terminated recall by Stryker Howmedica Osteonics Corp., reported 2013-01-16, distributed nationwide. Stryker has received a report that single size 3.5 stem was packaged as size 2.5 stem resulting in a possible
| Recall number | Z-0656-2013 |
|---|---|
| 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 | 2012-10-23 |
| Classified | 2013-01-08 |
| Reported by FDA | 2013-01-16 |
| Terminated | 2013-09-11 |
| Distributed | Nationwide (US) |
| Lot numbers | 40163005, 40264005 |
| Model numbers | 6021-2530, 6021-3535 |
Product
Accolade TMZF Plus 127 degree Neck Angle V40 Hip Stem #2.5 and Accolade TMZF Plus 127 degree Neck Angle V40 Hip Stem #3.5, Howmedica Osteonics Corp. The intended use is for reconstruction of the head and neck of the femoral joint.
Reason for recall
Stryker has received a report that single size 3.5 stem was packaged as size 2.5 stem resulting in a possible product mix.
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-0656-2013. 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.