FDA Device recall Z-0371-2024
Compress Device Segmental Anchor Plug, 12 MM -For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacem…
- FDA Device
- Class II
- ongoing
- Published 2023-11-29
On 2023-11-29 the FDA classified a Class II recall of Compress Device Segmental Anchor Plug, 12 MM -For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacem… by Biomet, citing anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0371-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-10-09 |
| Published | 2023-11-29 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Biomet |
| Distribution | US |
Product
Compress Device Segmental Anchor Plug, 12 MM -For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178402
Reason
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Identifiers
| code_info | Lot Numbers/UDI 240750 (01)00880304259713(17)270112(10)240750 671330 (01)00880304259713(17)271114(10)671330 671420…Lot Numbers/UDI 240750 (01)00880304259713(17)270112(10)240750 671330 (01)00880304259713(17)271114(10)671330 671420 (01)00880304259713(17)270831(10)671420 671660 (01)00880304259713(17)270901(10)671660 752730 (01)00880304259713(17)270802(10)752730 752760 (01)00880304259713(17)270816(10)752760 798010 (01)00880304259713(17)270120(10)798010 921660 (01)00880304259713(17)270724(10)921660 930670 (01)00880304259713(17)270727(10)930670 930680 (01)00880304259713(17)270802(10)930680 965330 (01)00880304259713(17)271112(10)965330 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0371-2024%22
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