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HomeBECTON, DICKINSON AND COMPANY › BD BBL™ Modified Thayer-Martin (MTM II) Agar

BD BBL™ Modified Thayer-Martin (MTM II) Agar

BECTON, DICKINSON AND COMPANY · Model 221567 · UDI-DI 10382902215674

JTY Prescription
1
510(k) clearances
82
Adverse events
9
Recalls
6
Facilities

Description

Plate Thayer-Martin Mod MTM II 20 Ea

Recalls

DateFirmReason
2026-06-03Remel, IncReduced or no recovery of some strains of Neisseria gonorrhoeae.
2022-11-21Becton Dickinson & Co.Boxes contain a reduced concentration of Nicotinamide Adenine Dinucleotide and does not provide enough of the blood factors necessary to support Haemophilus growth. The reduction c
2021-03-17Becton Dickinson & Co.Products show heavy growth of C. albicans after 24 hours of incubation due to misformulation (expected reaction is partial inhibition after 18-48 hours incubation) and reduce the
2021-03-17Becton Dickinson & Co.Products show heavy growth of C. albicans after 24 hours of incubation due to misformulation (expected reaction is partial inhibition after 18-48 hours incubation) and reduce the
2018-06-21Becton Dickinson & Co.A portion of this lot was manufactured using Gentamicin instead of Vancomycin. Gentamicin is an inhibitory agent of Neisseria organisms. This product is a selective plated medium t
2013-02-08Becton Dickinson & Co.Increased levels of false positives in BD Probe Tech Neisseria gonorrhoeae Q Amplified DNA assay kits.
2003-10-10Becton Dickinson & CoMicrobiological media may exhibit reduced colony size of bacteria, Haemophilus species.
2003-10-02Remel, IncSome of the product lots exhibit no growth of quality control strains of Neisseria gonorrhoeae
2002-11-18Becton Dickinson & Co.Microbiological media may exhibit No Growth or reduced colony size of Haemophilus species.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.