# FDA recall Z-1410-2022

> **Aesculap Implant Systems LLC** · Class II · device recall initiated 2021-10-25.

## 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.

## Distribution

US: CA, FL, GA, IL, OH & MI

## Key facts

- **Recall number:** Z-1410-2022
- **Recalling firm:** Aesculap Implant Systems LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-10-25
- **Report date:** 2022-07-27
- **Termination date:** 2024-06-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Center Valley, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1410-2022

## Citation

> AI Analytics. FDA recall Z-1410-2022. Retrieved 2026-07-12 from https://api.ai-analytics.org/recall/Z-1410-2022. Source: US FDA. Licensed CC0.

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