# FDA recall Z-1477-2024

> **Wright Medical Technology, Inc.** · Class II · device recall initiated 2024-03-06.

## Product

stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty

## Reason for recall

Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal screw in the finished instrument assembly. The missing screw is used to lockout the Medial/Lateral adjustment on the INFINITY Resection Adjustment Guide.

## Distribution

US: TX, NE, and  AUSTRALIA, BELGIUM, BRAZIL, CANADA, CHINA, COLOMBIA, FRANCE, GERMANY, ITALY, SPAIN, SWEDEN, SWITZERLAND, UK

## Key facts

- **Recall number:** Z-1477-2024
- **Recalling firm:** Wright Medical Technology, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-06
- **Report date:** 2024-04-10

- **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-1477-2024

## Citation

> AI Analytics. FDA recall Z-1477-2024. Retrieved 2026-08-02 from https://api.ai-analytics.org/recall/Z-1477-2024. Source: US FDA. Licensed CC0.

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