Becton Dickinson & Co. 2024-10-02 Health serious FDA
Health · FDA · Recall #FDA-Z-3246-2024
BD Phoenix M50 instrument -Intended for the rapid identification (ID) and antimicrobial… Recall
Issued October 2, 2024 · Becton Dickinson & Co.
In October 2024, Becton Dickinson & Co. recalled the BD Phoenix M50 instrument -Intended for the rapid identification (ID) and antimicrobial…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Escherichia coli (E. coli) misidentification for clinical samples that were tested on BD Phoenix" M50 instrument and BD Phoenix" 100, may lead to misdiagnosis and inappropriate treatment of infections caused by E. coli,
What you should do
- 1 Stop using BD Phoenix M50 instrument -Intended for the rapid identification (ID) and antimicrobial… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Becton Dickinson & Co. 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 & Co.
- Category
- Health
- Recall date
- October 2, 2024
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of Algeria, Argentina, Armenia, Australia, Austria, Azerbaijan, Bahrain, Bangladesh
- Recall number
- FDA-Z-3246-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Becton Dickinson & Co. has 7 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.