FDASeptember 1, 2022device

Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or arterial access.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Potential for leakage at the catheter hub.

What to do

FDA enforcement status: Ongoing

Brands named

b braun medical

UPCs

04046963318154

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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