BD GasPak™ EZ Campy Gas Generating Pouch System 260685Recalls & reported problems
Becton, Dickinson And Company · BD GasPak™ EZ Campy Gas Generating Pouch System · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Apr 7, 2026Class IIOpen, Classified
BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide levels below specification.
Z-1983-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
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 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
- 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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