BD BBL™ DrySlide™ Oxidase 231746Recalls & reported problems
Becton, Dickinson And Company · BD BBL™ DrySlide™ Oxidase · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 30382902317464), received between Mar 31, 2023 and Oct 17, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “False Positive Result” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- False Positive Result2
- Incorrect, Inadequate or Imprecise Result or Readings1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 17, 2023Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED THAT WHILE USING BD BBL¿ DRYSLIDE¿ OXIDASE, COLOR CHANGE WAS NOT OBSERVABLE BY OXIDASE POSITIVE ORGANISM PSEUDOMONAS. NO PATIENT IMPACT REPORTED. "TEST PERFORMS NOT AS EXPECTED: COLOR CHANGE WAS NOT OBSERVABLE BY OXIDASE POSITIVE ORGANISM (PSEUDOMONAS) , IT REMAINED COLORLESS DURING USE WERE PATIENT SAMPLES INVOLVED?: YES".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17953732 ↗MalfunctionMay 30, 2023False Positive Result; False Positive Result
IT WAS REPORTED THAT BD BBL¿ DRYSLIDE¿ OXIDASE 2 STRAIN TESTS CAME BACK POSITIVE BUT SHOULD BE NEGATIVE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE MEDIA ARE COLUMBIA BIOMÉRIEUX AND THE STRAINS ARE ATCC REFERENCE STRAINS ALL 3 STRAINS ARE POSITIVE IN LESS THAN 20 SECONDS WHILE E.COLI AND K. PNEUMONIAE SHOULD BE NEGATIVE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17020624 ↗MalfunctionMar 31, 2023False Positive Result; False Positive Result
IT WAS REPORTED THAT WHILE USING THE BD BBL¿ DRYSLIDE¿ OXIDASE THAT THERE WAS FALSE POSITIVES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: BATCH WITH FALSE POSITIVE OXIDASE TEST RESULTS. THE E COLI 25922 QUALITY CONTROL GIVES A POSITIVE REACTION IN LESS THAN 20 SECONDS (EXPECTED NEGATIVE RESULT). THE REAGENT IS STORED UNDER THE RECOMMENDED CONDITIONS AND EVEN WHEN OPENING A NEW CARD THERE IS A FLUCTUATION IN THE TEST RESPONSE. THE PROBLEMS SEEM TO BE QUITE RANDOM BUT ALSO PRESENT ON SOME CLINICAL STRAINS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16655379 ↗
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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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