BD BACTEC Plus Aerobic/F Culture Vials — Class II medical device recall Z-0110-2024
Ongoing recall by Becton Dickinson & Co., reported 2023-10-18, distributed nationwide. Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling issue where duplicate barcode seq
| Recall number | Z-0110-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Co., Sparks, MD, United States |
| Recall initiated | 2023-09-12 |
| Classified | 2023-10-12 |
| Reported by FDA | 2023-10-18 |
| Distributed | Nationwide (US) |
| Quantity | 781,600 vials |
| Reason classes | labeling |
| Lot numbers | 3062843, 3062846, 3062847, 3062849, 3067488, 3067489 |
| Model numbers | 442023 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0110-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.