Command Instrument Broach Handle — Class II medical device recall Z-0919-2013
Terminated recall by Stryker Howmedica Osteonics Corp., reported 2013-03-20, distributed nationwide. Reports of handle fracture and subsequent disassociation of cam assembly subcomponents during use.
| Recall number | Z-0919-2013 |
|---|---|
| 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 | 2012-12-20 |
| Classified | 2013-03-08 |
| Reported by FDA | 2013-03-20 |
| Terminated | 2015-09-30 |
| Distributed | Nationwide (US) |
| Quantity | 48 units |
| Reason classes | device malfunction |
| Lot numbers | RD5T305, RD5T305A, RD5T305L, RD5T305M, RD5T305T, RD5T306, RD5T306X, RD5T307, RD6W017, RD6W017A, RD6W017J, RD7L234, RD7L234X, RD7L235 |
| Model numbers | 6266-0-100 |
Product
Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog Number: 6266-0-100
Reason for recall
Reports of handle fracture and subsequent disassociation of cam assembly subcomponents during use.
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-0919-2013. 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.