FDA Device recall Z-2073-2017
Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
- FDA Device
- Class II
- terminated
- Published 2017-05-24
On 2017-05-24 the FDA classified a Class II recall of Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600 by Biomet Microfixation, citing part of the number on the tray lid differ from the part number on the base.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2073-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-04-11 |
| Published | 2017-05-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Biomet Microfixation |
| Distribution | AL, MO, UT |
Product
Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
Reason
Part of the number on the tray lid differ from the part number on the base.
Identifiers
| code_info | Part Number 46-1610 // Lot Number 709730 Part Number 46-1610 // Lot Number 709740 Part Number 46-1620 // Lot Number 7…Part Number 46-1610 // Lot Number 709730 Part Number 46-1610 // Lot Number 709740 Part Number 46-1620 // Lot Number 709710 Part Number 46-1620 // Lot Number 709720 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2073-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.