BD BBL™ GasPak™ 100 Anaerobic System 260626Recalls & reported problems
Becton, Dickinson And Company · BD BBL™ GasPak™ 100 Anaerobic System · Class 1
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 00382902606260), received between Mar 9, 2023 and Mar 9, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (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
- Incorrect, Inadequate or Imprecise Result or Readings1
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.
MalfunctionMar 9, 2023Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED THAT BD BBL¿ GASPAK¿ 100 ANAEROBIC SYSTEM EXPERIENCING GROWTH ISSUES WHEN USING GASPAK SYSTEM. NO INJURIES WERE REPORTED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CUSTOMER REPORTED THEY ARE EXPERIENCING GROWTH ISSUES WHEN USING THE GASPAK SYSTEM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16513363 ↗
Other DEVICE, GAS GENERATING devices
- BD GasPak™ EZ CO2 Gas Generating Pouch System 260684Becton, Dickinson And Company · DEVICE, GAS GENERATING1 recall4 reports
- BD GasPak™ EZ Campy Gas Generating Pouch System 260685Becton, Dickinson And Company · DEVICE, GAS GENERATING1 recall0 reports
- 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™ CO2 Indicators 271055Becton, Dickinson And Company · DEVICE, GAS GENERATING1 report
- BD GasPak™ EZ Campy Container System Sachets 260680Becton, 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page