MODULIFT VBR SZ — Class II medical device recall Z-1410-2022
Terminated recall by Aesculap Implant Systems LLC, reported 2022-07-27, distributed in CA, FL, GA, IL, MI, OH. Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant
| Recall number | Z-1410-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aesculap Implant Systems LLC, Center Valley, PA, United States |
| Recall initiated | 2021-10-25 |
| Classified | 2022-07-19 |
| Reported by FDA | 2022-07-27 |
| Terminated | 2024-06-12 |
| Distributed | CA, FL, GA, IL, MI, OH |
| Quantity | 9 units |
| UPC / GTIN / UDI-DI | 04046964067648 |
Product
MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441
Reason for recall
Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant.
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-1410-2022. 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.