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Recall Observatory FDA recall evidence

Device 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

Z-1482-2026

February 02, 2026

Class II

Product summary

Firm
B Braun Medical Inc
Event
Event 98380
Status
Ongoing
Classification
Class II
Quantity
21000 units
Official record key
device-enforcement:Z-1482-2026

Official wording

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

Code information: 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

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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