BD BBL™ CO2 Indicators 271055Recalls & reported problems
Becton, Dickinson And Company · BD BBL™ CO2 Indicators · Class 1
Data updated Oct 16, 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 30382902710555), received between Dec 10, 2021 and Dec 10, 2021 — 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 16, 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.
MalfunctionDec 10, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT WHILE USING BD GASPAK¿ CO2 INDICATORS INCORRECT LABEL INFORMATION WAS OBSERVED BY THE LABORATORY PERSONNEL. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "EXPIRY ON PRODUCT DOES NOT MATCH CERTIFICATE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12978267 ↗
Other DEVICE, GAS GENERATING devices
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- BD GasPak™ EZ Anaerobe Gas Generating Pouch System with Indicator 260683Becton, Dickinson And Company · DEVICE, GAS GENERATING4 reports
- BD GasPak™ EZ Anaerobe Container System Sachets with Indicator 260001Becton, Dickinson And Company · DEVICE, GAS GENERATING3 reports
- BD GasPak™ EZ Anaerobe Container System Sachets 260678Becton, Dickinson And Company · DEVICE, GAS GENERATING2 reports
- BD BBL™ Dry Anaerobic Indicator Strips 271051Becton, Dickinson And Company · DEVICE, GAS GENERATING1 report
- BD BBL™ Bio-Bag™ Environmental Chamber Type C 261212Becton, Dickinson And Company · DEVICE, GAS GENERATING1 report
- BD BBL™ GasPak™ 100 Anaerobic System 260626Becton, Dickinson And Company · DEVICE, GAS GENERATING1 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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