# FDA recall Z-0113-2024

> **Tornier, Inc** · Class II · device recall initiated 2023-09-15.

## Product

stryker Tornier Perform Reversed Augmented Glenoid Lateralized Baseplate, 25mm, Offset +3mm, REF DWJ502

## Reason for recall

One lot of Tournier Perform Reversed Lateralized Baseplates were found to have been manufactured with 6mm spacers instead of 3mm spacers. This nonconformance prevents the central screw from being able to thread into the baseplate.

## Distribution

US:  CA, CO, IL, MA, MN, NC, OR, RI, SC, TN

## Key facts

- **Recall number:** Z-0113-2024
- **Recalling firm:** Tornier, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-15
- **Report date:** 2023-10-25

- **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-0113-2024

## Citation

> AI Analytics. FDA recall Z-0113-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0113-2024. Source: US FDA. Licensed CC0.

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