FDA Device recall Z-1401-2023
MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device
- FDA Device
- Class II
- completed
- Published 2023-04-26
On 2023-04-26 the FDA classified a Class II recall of MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device by Medacta Usa, citing there is a potential for breakage of the small screw used to affix the anti-backout plate.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1401-2023 |
| Classification | Class II |
| Status | completed |
| Initiated | 2023-03-08 |
| Published | 2023-04-26 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medacta Usa |
| Distribution | AZ, GA, ID, TX, VA |
Product
MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device
Reason
There is a potential for breakage of the small screw used to affix the anti-backout plate.
Identifiers
| code_info | UDI/DI 07630345732293, All Lot Numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1401-2023%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.