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B Braun Medical Inc recalls Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or arteri
Recalled October 12, 2022 · FDA recall Z-0009-2023 · B Braun Medical
Hazard
Potential for leakage at the catheter hub. · FDA Class II
Units
94,000 US
Sold at
Domestic distribution to AZ CA FL GA MD MI MO MS NC NY OH PA TN TX WA. Foreign distribution to Canada
Description
Potential for leakage at the catheter hub.
Product
Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or arterial access.
Manufacturer(s)
B Braun Medical Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →