BD BACTEC Plus Aerobic/F Culture Vials recall: Labeling Error
BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023
Why was BD BACTEC Plus Aerobic/F Culture Vials 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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI: 038290HXRPGWNNMN; Lot Numbers: 3062843 3062846 3062849 3062847 3067489 3067488
- Product
- BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023
- Recalling firm
- Becton Dickinson & Co.
- Quantity
- 781,600 vials
- Distribution
- Worldwide - US Nationwide distribution.
- Recall date
- October 18, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)