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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

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 ↗

Other DISCS, STRIPS AND REAGENTS, MICROORGANISM DIFFERENTIATION devices

All DISCS, STRIPS AND REAGENTS, MICROORGANISM DIFFERENTIATION devices →

Sources and updates

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