MectaLIF ANTERIOR — Class II medical device recall Z-1403-2023
Completed recall by Medacta Usa Inc, reported 2023-04-26, distributed in AZ, GA, ID, TX, VA. There is a potential for breakage of the small screw used to affix the anti-backout plate.
| Recall number | Z-1403-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medacta Usa Inc, Memphis, TN, United States |
| Recall initiated | 2023-03-08 |
| Classified | 2023-04-19 |
| Reported by FDA | 2023-04-26 |
| Distributed | AZ, GA, ID, TX, VA |
| Quantity | 34 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 07630345732316 |
| Model numbers | 03.30.303 |
Product
MectaLIF ANTERIOR - Lag Plate Flush H16, REF 03.30.303, interbody fusion device
Reason for recall
There is a potential for breakage of the small screw used to affix the anti-backout plate.
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-1403-2023. 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.