Becton Dickinson & Company 2022-07-27 Health serious FDA
Health · FDA · Recall #FDA-Z-1433-2022
BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS) Recall
Issued July 27, 2022 · Becton Dickinson & Company
In July 2022, Becton Dickinson & Company recalled the BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS), a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under dosing/under infusion, contamination and/or air ingress.
What you should do
- 1 Stop using BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS) right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Becton Dickinson & Company 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
- Becton Dickinson & Company
- Category
- Health
- Recall date
- July 27, 2022
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide distribution in the states of AK, AR, AZ, CA, CO, FL, GA, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC, NE,
- Recall number
- FDA-Z-1433-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Becton Dickinson & Company has 6 recalls in our database, including 2 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.