B Braun Medical Inc 2022-10-12 Health serious FDA
Health · FDA · Recall #FDA-Z-0009-2023
Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle… Recall
Issued October 12, 2022 · B Braun Medical Inc
In October 2022, B Braun Medical Inc recalled the Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Potential for leakage at the catheter hub.
What you should do
- 1 Stop using Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact B Braun Medical Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- B Braun Medical Inc
- Category
- Health
- Recall date
- October 12, 2022
- Units affected
- Not reported
- Sold at
- Domestic distribution to AZ CA FL GA MD MI MO MS NC NY OH PA TN TX WA. Foreign distribution to Canada
- Recall number
- FDA-Z-0009-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- B Braun Medical Inc has 23 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.