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B Braun Medical Inc recalls Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A
Recalled March 11, 2026 · FDA recall Z-1482-2026 · B Braun Medical
Hazard
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break. · FDA Class II
Units
21000 units
Sold at
Worldwide - US Nationwide distribution in the state of TX and the country of Costa Rica.
Description
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
Product
Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 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
Manufacturer(s)
B Braun Medical Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →