Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm — Class II medical device recall Z-1242-2014
Terminated recall by Biomet, Inc., reported 2014-03-26, distributed nationwide. Incorrect labeling on specific lots of the Intramedullary Bone Saw.The Saw Blade Assembly was identified as CA
| Recall number | Z-1242-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2014-02-26 |
| Classified | 2014-03-20 |
| Reported by FDA | 2014-03-26 |
| Terminated | 2015-07-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, NL |
| Quantity | 1 |
| Reason classes | labeling |
| Lot numbers | 669420 |
| Model numbers | 475620 |
Product
Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm, A unique and exclusive clinical instrument used to correct leg length, or rotational discrepancies in the femur.
Reason for recall
Incorrect labeling on specific lots of the Intramedullary Bone Saw.The Saw Blade Assembly was identified as CAM Assembly.
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-1242-2014. 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.