Class II

Medical Device Recall: stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty

Wright Medical Technology, Inc. · March 6, 2024

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

States Affected

NE, TX

Quantity Affected

47 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1477-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Wright Medical Technology, Inc. Medical Device Recall: stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty | SafeCheck