Recall archive / FDA device enforcement
MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441 — FDA record Z-1410-2022
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Oct 25, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- 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.
- Classification
- Class II
- Recalling firm
- Aesculap Implant Systems LLC
- Quantity
- 9 pieces
- Agency-reported status
- Terminated
- Source record identifier
- Z-1410-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI-DI: 04046964067648 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US: CA, FL, GA, IL, OH & MI
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Jul 27, 2022
- Recall initiation date
- Oct 25, 2021
- Center classification date
- Jul 19, 2022
- Termination date
- Jun 12, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.