# FDA recall Z-0773-2024

> **Tornier, Inc** · Class II · device recall initiated 2024-01-03.

## Product

Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V, REF DWJ001, L: 7mm, Cementless Sterile.

## Reason for recall

The incorrect device is contained in the labeled package.

## Distribution

Distribution was made to AR, AZ, CA, CO, CT, NC, OH, TN, and VA.  There was no military/government distribution.  Foreign distribution was made to Australia, France, and Italy.

## Key facts

- **Recall number:** Z-0773-2024
- **Recalling firm:** Tornier, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-01-03
- **Report date:** 2024-01-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bloomington, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0773-2024

## Citation

> AI Analytics. FDA recall Z-0773-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0773-2024. Source: US FDA. Licensed CC0.

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