Medical Device Recall: Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be us
B Braun Medical Inc · February 2, 2026
Reason for Recall
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
Product Description
Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A
Distribution
Worldwide - US Nationwide distribution in the state of TX and the country of Costa Rica.
States Affected
NATIONWIDE
Quantity Affected
51300 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1483-2026
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.