Home › Device types › MDB
System, Blood Culturing
FDA product code MDB · Class 1 · Microbiology
90
Registered devices
6,354
Adverse events
76
Recalls
68
510(k) clearances
Devices with this code
VersaTREK — REMEL, INC.BD BACTEC™ 9240 — BECTON, DICKINSON AND COMPANYBACT/ALERT® SA — BIOMERIEUX , INC.BD BACTEC™ PANTA™/F — BECTON, DICKINSON AND COMPANYBD BACTEC™ Plus Aerobic/F Culture Vials — BECTON, DICKINSON AND COMPANYBACT/ALERT® 3D LEFT COMBINATION MODULE — BIOMERIEUX , INC.BACT/ALERT® FA PLUS — BIOMERIEUX , INC.BD BACTEC™ Plus Anaerobic/F Culture Vials — BECTON, DICKINSON AND COMPANYVERSATREK 240 W/4 DR/CTRL MOD, 220V — REMEL, INC.BacT/ALERT®3D — BIOMERIEUX , INC.BD BACTEC™ MGIT™ 960 Calibration Vial — BECTON, DICKINSON AND COMPANYBD BACTEC™ MGIT™ 960 Instrument — BECTON, DICKINSON AND COMPANYVERSATREK 528 W/18 DR/CTRL MOD 220V — REMEL, INC.BD BACTEC™ Peds Plus™/F Culture Vials — BECTON, DICKINSON AND COMPANYBD BACTEC™ 9120, Remanufactured — BECTON, DICKINSON AND COMPANYVersaTREK™ — REMEL, INC.NA — REMEL, INC.BD BACTEC™ Supplement/F — BECTON, DICKINSON AND COMPANYVERSATREK 240 W/4 DRAWERS/CTRL MOD — REMEL, INC.BD BACTEC™ Lytic/10 Anaerobic/F Culture Vials — BECTON, DICKINSON AND COMPANYBACT/ALERT® FA — BIOMERIEUX , INC.BD BACTEC™ 9240, Remanufactured — BECTON, DICKINSON AND COMPANYBD BACTEC™ MGIT™ 320 Instrument — BECTON, DICKINSON AND COMPANYNA — REMEL, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-09-23 | Becton Dickinson & Co. | Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product se |
| 2025-09-23 | Becton Dickinson & Co. | Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product se |
| 2024-10-31 | Becton Dickinson & Co. | BD confirmed that product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Unti |
| 2024-10-31 | Becton Dickinson & Co. | BD confirmed that product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Unti |
| 2024-10-31 | Becton Dickinson & Co. | BD confirmed that product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Unti |
| 2024-10-31 | Becton Dickinson & Co. | BD confirmed that product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Unti |
| 2023-09-12 | Becton Dickinson & Co. | 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 on |
| 2018-06-27 | bioMerieux, Inc. | The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of the four (4) resident calibration standards so that Field System Engineers (FSE) can |
| 2018-06-27 | bioMerieux, Inc. | The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of the four (4) resident calibration standards so that Field System Engineers (FSE) can |
| 2018-06-27 | bioMerieux, Inc. | The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of the four (4) resident calibration standards so that Field System Engineers (FSE) can |
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