Hoffman LRF Wire Bolt — Class II medical device recall Z-0695-2013
Terminated recall by Stryker Howmedica Osteonics Corp., reported 2013-01-23, distributed nationwide. Two complaints have been filed where Hoffman LRF Wires have broken during load bearing application by patients
| Recall number | Z-0695-2013 |
|---|---|
| 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 | 2012-10-25 |
| Classified | 2013-01-17 |
| Reported by FDA | 2013-01-23 |
| Terminated | 2015-12-01 |
| Distributed | Nationwide (US) |
| Quantity | 476 units |
| Lot numbers | Z02804, Z08348, Z08349, Z08350, Z08351, Z09344, Z12549, Z12551, Z12554, Z16246, Z16752, Z16753, Z16996 |
| Model numbers | 4933-1-001, 4933-1-002, 4933-1-003 |
Product
Hoffman LRF Wire Bolt, Catalog number 4933-1-001 through -003.
Reason for recall
Two complaints have been filed where Hoffman LRF Wires have broken during load bearing application by patients.
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-0695-2013. 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.