Class II — Biomet Microfixation, LLC
| Recalling firm | BIOMET MICROFIXATION |
|---|---|
| Registered facility | BIOMET MICROFIXATION (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Part of the number on the tray lid differ from the part number on the base. |
| Product | Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600 |
| Quantity | 33 units |
| Distribution | AL, MO and UT Canada, Australia, Netherlands, and Egypt |
| Initiated | 2017-04-11 |
| Classified | 2017-05-12 |
| Terminated | 2019-08-06 |
| Recall number | Z-2073-2017 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Biomet Microfixation, LLC (Z-2073-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/77022/
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