Home › Device types › MJA
Susceptibility Test Powders, Antimycobacterial
FDA product code MJA · Class 2 · Microbiology
7
Registered devices
874
Adverse events
6
Recalls
5
510(k) clearances
Devices with this code
BD BACTEC™ MGIT™ 960 STR 4.0 Kit — BECTON, DICKINSON AND COMPANYNA — REMEL, INC.BD BACTEC™ MGIT™ 960 SIRE Kit — BECTON, DICKINSON AND COMPANYBD BACTEC™ MGIT™ 960 INH 0.4 Kit — BECTON, DICKINSON AND COMPANYBD BACTEC™ MGIT™ 960 IR Kit — BECTON, DICKINSON AND COMPANYBD BACTEC™ MGIT™ 960 PZA Kit — BECTON, DICKINSON AND COMPANYBD BACTEC™ MGIT™ 960 PZA Medium — BECTON, DICKINSON AND COMPANY
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-05-20 | Becton Dickinson & Co. | BD has received additional complaints of intermittent false resistance results for PZA during susceptibility testing of Mycobacterium tuberculosis isolates. |
| 2024-07-18 | Becton Dickinson & Co. | May intermittently produce falsely resistant results for pyrazinamide (PZA) during susceptibility testing of Mycobacterium tuberculosis isolates. |
| 2010-08-31 | Becton Dickinson & Co. | In vitro diagnostic device components are mislabeled. |
| 2010-08-31 | Becton Dickinson & Co. | In vitro diagnostic device components are mislabeled. |
| 2010-08-31 | Becton Dickinson & Co. | In vitro diagnostic device components are mislabeled. |
| 2010-08-31 | Becton Dickinson & Co. | In vitro diagnostic device components are mislabeled. |
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