Medicrea TLIF-B Holder — Class II medical device recall Z-1156-2020
Terminated recall by Medicrea International, reported 2020-02-19, distributed in OH, VA. Inner draw rod, which threads into the cage may potentially be separated from the proximal knob of the inserte
| Recall number | Z-1156-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medicrea International, Rillieux La Pape, France |
| Recall initiated | 2019-10-02 |
| Classified | 2020-02-12 |
| Reported by FDA | 2020-02-19 |
| Terminated | 2021-02-08 |
| Distributed | OH, VA |
| Quantity | 14 units |
| Lot numbers | 19B0572, L9B0570 |
| Model numbers | A24200010 |
Product
Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010
Reason for recall
Inner draw rod, which threads into the cage may potentially be separated from the proximal knob of the inserter
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-1156-2020. 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.