---
title: "MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium I... — FDA record Z-1410-2022 | Is It on Recall"
description: "Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant."
url: https://isitonrecall.com/recall/fda-device-z-1410-2022-modulift-vbr-sz-m-4mm-set-screw-driver-mf790r-part-of-modulift-vbr-medium-instrument-set-st-0441/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / 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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## 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

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1410-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). 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.

- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [Ohio](https://isitonrecall.com/state/ohio/)

## 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.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1410-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Aesculap Implant Systems LLC records](https://isitonrecall.com/brand/aesculap-implant-systems-llc/)