Recall
FDAHealthFebruary 2, 2026

B Braun Medical Inc — 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

⚠️ The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
February 2, 2026

Worldwide - US Nationwide distribution in the state of TX and the country of Costa Rica.

What's affected?

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
Lot code
0062004706

Additional details

Model/Catalog Number: 7A3842; Primary-DI 4046964338434; Unit of Use- DI 4046964338410; Lot 0062004706, Exp 31MAR2032; Lot 0062005799, Exp 30JUN2032; Lot 0062006415, Exp 31MAR2032; Lot 0062006416, Exp 31MAR2032; Lot 0062023397, Exp 30JUN2032; Lot 0062024887, Exp 31JUL2032

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 21000 units.

View original FDA notice →

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