BD Difco™ Mueller Hinton Agar 225250Recalls & reported problems
Becton, Dickinson And Company · BD Difco™ Mueller Hinton Agar · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382902252504), received between Sep 1, 2023 and Sep 1, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Markings/Labelling Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Device Markings/Labelling Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 1, 2023Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT WHILE USING BD DIFCO¿ MUELLER HINTON AGAR THAT THERE WAS THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER THAT THERE WAS NO LABEL OR MISSING LABEL INFORMATION. 'WE RECEIVED BD MUELLER HINTON REF. 225250 BUT IT ISN¿T CE MARKED AS EXPECTED? THE LABEL MENTIONS ¿FOR LAB USE ONLY¿ BUT FOR HUMAN CLINICAL IT WOULD NEED TO BE CE MARKED. I THOUGHT THAT I WOULD RECEIVE PRODUCT WITH THE NEW LABEL WHICH IS MULTI FOLDED TO ALLOW THEM TO HAVE ALL EUROPEAN LANGUAGES INCLUDING PREPARATION INSTRUCTIONS."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17671273 ↗
Other CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGAR/BROTH devices
- NA CP114-10Remel, Inc. · Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth1 recall0 reports
- BD BBL™ Mueller Hinton II Agar 221800Becton, Dickinson And Company · CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGAR/BROTH11 reports
- BD BBL™ Mueller Hinton II Agar 211438Becton, Dickinson And Company · CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGAR/BROTH3 reports
- BD BBL™ Mueller Hinton II Agar 221275Becton, Dickinson And Company · CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGAR/BROTH3 reports
- BD BBL™ Mueller Hinton II Broth, Cation-Adjusted 212322Becton, Dickinson And Company · CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGAR/BROTH2 reports
- BD BBL™ Mueller Hinton II Agar 212257Becton, Dickinson And Company · CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGAR/BROTH1 report
- BD BBL™ Mueller Hinton II Agar 221177Becton, Dickinson And Company · CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGAR/BROTH1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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