Biomet Parsippany — Class II medical device recall Z-2744-2015
Terminated recall by Biomet Spine, LLC, reported 2015-09-16, distributed nationwide. Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.
| Recall number | Z-2744-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet Spine, LLC, Broomfield, CO, United States |
| Recall initiated | 2015-08-05 |
| Classified | 2015-09-09 |
| Reported by FDA | 2015-09-16 |
| Terminated | 2016-02-10 |
| Distributed | Nationwide (US) |
| Quantity | 7 parts |
| Reason classes | labeling |
| Lot numbers | 375440 |
| Model numbers | 14-521614B |
Product
Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.
Reason for recall
Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.
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-2744-2015. 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.