BD GasPak™ EZ Campy Container System Sachets 260680Recalls & reported problems
Becton, Dickinson And Company · BD GasPak™ EZ Campy Container System Sachets · 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 30382902606803), received between May 4, 2026 and May 4, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “False Positive Result” (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.
Reports received per month
Most reported problems
Device problems
- False Positive Result1
- 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.
MalfunctionMay 4, 2026False Positive Result; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED THAT WHILE USING BD GASPAK¿ EZ CAMPY CONTAINER SYSTEM SACHETS, A FALSE POSITIVE RESULT WAS OBTAINED ON UNSPECIFIED NUMBER OF PATIENTS. THERE WAS NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25071616 ↗
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™ GasPak™ 100 Anaerobic System 260626Becton, Dickinson And Company · DEVICE, GAS GENERATING1 report
- BD BBL™ CO2 Indicators 271055Becton, 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.
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