Becton Dickinson & Co. Recall: BD BBL Sensi Disc Azithromycin -15 ¿g, Catalog Number 23168
Becton Dickinson & Co. Recall: BD BBL Sensi Disc Azithromycin -15 ¿g, Catalog Number 23168 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Becton Dickinson & Co.; Product: BD BBL Sensi Disc Azithromycin -15 ¿g, Catalog Number 231682¿used for semi-quantitative in vitro susceptibility te
| Recalling firm | Becton Dickinson & Co. |
|---|---|
| Product | BD BBL Sensi Disc Azithromycin -15 ¿g, Catalog Number 231682¿used for semi-quantitative in vitro susceptibility testing. |
| Reason for recall | There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or additional adverse diagnostic outcomes, such as a delay in diagnosis, the selection of inappropriate antibiotics, or extended duration of antibiotic exposure and the treatment process. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Domestic distribution nationwide. International distribution worldwide. |
| Recall initiated | 20240108 |
| Recall number | Z-1015-2024 |
| Category | device |
| State | MD |
| Country | United States |
$29/mo
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