FDA Device recall Z-0110-2024
BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023
- FDA Device
- Class II
- ongoing
- Published 2023-10-18
On 2023-10-18 the FDA classified a Class II recall of BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023 by Becton Dickinson And, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0110-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-09-12 |
| Published | 2023-10-18 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023
Reason
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.
Identifiers
| code_info | UDI-DI: 038290HXRPGWNNMN; Lot Numbers: 3062843 3062846 3062849 3062847 3067489 3067488 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0110-2024%22
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