Z-0110-2024 Class II Ongoing
FDA device recall Z-0110-2024 was initiated by Becton Dickinson & Co. on September 12, 2023 and is designated Class II. Reason for recall: 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. The recall status is ongoing. Affected quantity: 781,600 vials.
Recall Details
- Product Type
- Devices
- Report Date
- October 18, 2023
- Initiation Date
- September 12, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 781,600 vials
Product Description
BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023
Reason for Recall
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.
Distribution Pattern
Worldwide - US Nationwide distribution.
Code Information
UDI-DI: 038290HXRPGWNNMN; Lot Numbers: 3062843 3062846 3062849 3062847 3067489 3067488