FDA Device recall Z-1410-2022
MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441
- FDA Device
- Class II
- terminated
- Published 2022-07-27
On 2022-07-27 the FDA classified a Class II recall of MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441 by Aesculap Implant Systems, citing set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1410-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-10-25 |
| Published | 2022-07-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Aesculap Implant Systems |
| Distribution | CA, FL, GA, IL, MI, OH |
Product
MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441
Reason
Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant.
Identifiers
| code_info | UDI-DI: 04046964067648 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1410-2022%22
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