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FDA (Device enforcement)Recalled 2026-02-02class ii

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 impla

Hazard

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

Details from the source

Reason for recall: The potential for the needle tip to be dull/blunt, difficult to advance, and/or break. Distribution: Worldwide - US Nationwide distribution in the state of TX and the country of Costa Rica. Quantity: 21000 units Lot/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

UPC codes

4046964338434, 4046964338410

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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