# FDA recall Z-1941-2020

> **Medtronic Sofamor Danek USA Inc** · Class II · device recall initiated 2020-03-26.

## Product

VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628

## Reason for recall

Nonconforming product;  length of the product measured shorter than the labeled length.

## Distribution

US Nationwide distribution in the states of CA and MI.

## Key facts

- **Recall number:** Z-1941-2020
- **Recalling firm:** Medtronic Sofamor Danek USA Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-03-26
- **Report date:** 2020-05-20
- **Termination date:** 2021-03-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Memphis, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1941-2020

## Citation

> AI Analytics. FDA recall Z-1941-2020. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-1941-2020. Source: US FDA. Licensed CC0.

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