Biomet Microfixation TraumaOne System Surgical Tray — Class II medical device recall Z-2073-2017
Terminated recall by Biomet Microfixation, LLC, reported 2017-05-24, distributed in AL, MO, UT. Part of the number on the tray lid differ from the part number on the base.
| Recall number | Z-2073-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet Microfixation, LLC, Jacksonville, FL, United States |
| Recall initiated | 2017-04-11 |
| Classified | 2017-05-12 |
| Reported by FDA | 2017-05-24 |
| Terminated | 2019-08-06 |
| Distributed | AL, MO, UT |
| Countries outside the US | AU, CA, EG, NL |
| Quantity | 33 units |
| Lot numbers | 709710, 709720, 709730, 709740 |
| Model numbers | 46-1600, 46-1610, 46-1620 |
Product
Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
Reason for recall
Part of the number on the tray lid differ from the part number on the base.
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-2073-2017. 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.