WhichRecall
Class IIReported 2026-03-11

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

Recalled by B Braun Medical Inc

Reason for Recall

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

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Recall Number
Z-1482-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2026-02-02
Reported
2026-03-11
Distribution
Worldwide - US Nationwide distribution in the state of TX and the country of Costa Rica.
Code Info
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
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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