Reported Oct 18, 2023 · Ongoing
BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023
Becton Dickinson & Co.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Becton Dickinson & Co. · 7 Loveton Cir · Sparks, MD · 21152-9212
Is this the product you have?
- BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023
- Lot codes and dates
- UDI-DI038290HXRPGWNNMN
- Lot Numbers3062843 3062846 3062849 3062847 3067489 3067488
- Amount recalled
- 781,600 vials
Where it was sold
- Nationwide
Why it was recalled
Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling issue where duplicate barcode sequence numbers have been identified on more than one vial.
This product could cause temporary or reversible health problems — stop using it.
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