BD BBL™ Taxo™ V 231727Recalls & reported problems
Becton, Dickinson And Company · BD BBL™ Taxo™ Differentiation Discs V · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00382902317272), received between Jan 19, 2023 and Mar 16, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (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.
Most reported problems
Device problems
- Incorrect, Inadequate or Imprecise Result or Readings2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 16, 2023Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED THAT BD BBL¿ TAXO¿ DIFFERENTIATION DISCS FOR V FACTOR RESULT OF IDENTIFICATION WITH TAXO IS DISCREPANT WITH ONE BY MASS SPECTROMETRY. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: REPORT, THE RESULT OF AN IDENTIFICATION WITH TAXO IS DISCREPANT WITH THE ONE BY A MASS SPECTROMETRY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16552080 ↗MalfunctionJan 19, 2023Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED THAT 60 BD BBL¿ TAXO¿ DIFFERENTIATION DISCS FOR V FACTOR DURING VALIDATION NO GROWTH OCCURRED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: NO GROWTH OF HAEMOPHILUS INFLUENZAE AT THE EDGE OF 60 DISC WITH THE USE OF A COS + FACTOR V MEDIUM DURING VALIDATION NO GROWTH , ARE TESTING NOW WITH OTHER BATCH , TOMORROW NOON 11/1/2023 12H I HAVE TO CALL THE CUSTOMER FOR RESULTS OTHER BATCH.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16209274 ↗
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- RAPID ID 32 STREPBiomerieux SA · DISCS, STRIPS AND REAGENTS, MICROORGANISM DIFFERENTIATION5 reports
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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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