Drug recall
BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570
FDA recall event 95636 · Class II · Becton Dickinson & Co.
Key facts
| Event ID | 95636 |
|---|---|
| Recall numbers | Z-0584-2025, Z-0585-2025, Z-0586-2025, Z-0587-2025, Z-0588-2025, Z-0589-2025, Z-0590-2025, Z-0591-2025, Z-0592-2025, Z-0593-2025, Z-0594-2025, Z-0595-2025 and 1 more |
| Recalling firm | Becton Dickinson & Co. |
| Product type | Devices |
| Products | BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570, BACTEC 9240 System Version or Model: 445475 Catalog Number: 445475, BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296, BD BACTEC FX, Instrument Top, Packaged Version or Model: 441385 Catalog Number: 441385, BD COR GX Instrument Version or Model: 443990 Catalog Number: 443990 and 8 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | BD confirmed that product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are… |
| Initiation date | Oct 31, 2024 |
| Report date | Dec 11, 2024 |
| City | Sparks |
| State | MD |
| Country | United States |
| FEI number | 1119779 |
At a glance
- 10–99 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: