Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Introcan Safety FEP 14G Recalled by B Braun Medical Inc Due to Potential for leakage at the catheter hub.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact B Braun Medical Inc directly.
Affected Products
Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or arterial access.
Quantity: 94,000 US
Why Was This Recalled?
Potential for leakage at the catheter hub.
Where Was This Sold?
This product was distributed to 15 states: AZ, CA, FL, GA, MD, MI, MS, MO, NY, NC, OH, PA, TN, TX, WA
About B Braun Medical Inc
B Braun Medical Inc has 148 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report