FDA Device Intelligence
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Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth

FDA product code JTZ · Class 2 · Microbiology

72
Registered devices
106
Adverse events
8
Recalls
74
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-11-12Remel, IncProducts may contain contamination, which may result in a darker or brown media color.
2018-05-04Thermo FisherProduct may fail performance testing for S aureus ATCC 43300.
2017-11-02Remel IncProduct may have incorrect cation information detailed on the product label.
2011-04-20Becton Dickinson & Co.Oxacillin Screen Agar may not have been produced according to specification and could result in false antibiotic susceptibility test results in patient specimen
2009-12-08Remel, IncThe product may fail to adequately grow methicillin resistant Staphylococcus aureus ATCC 43300 and Staphylococcus aureus ATCC 33591.
2009-06-04Trek Diagnostic SystemsThirty-one boxes of unapproved quarantine product, CP112-10 MHB w/LHB, Lot # 150444SA, were inadvertently shipped to customers on 6/2/09 instead of shipping app
2008-09-22Trek Diagnostic SystemsIncorrect result: The absorbance has changed as the standards have aged; the standards' turbidity has become denser. The recalled lot is now reading 0.15 ABS @
2005-07-28Becton Dickinson & Co.Microbiological media for antibiotic susceptibility testing gives false test results.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.