AirLife CC10Recalls & reported problems
Carefusion Corporation · Airlife™ Nebulizer Cap · Class 2
All models of AirLife (23)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10885403199141), received between Jan 10, 2020 and Aug 7, 2020 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Infusion or Flow Problem” (3 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 16, 2026.
Most reported problems
Device problems
- Infusion or Flow Problem3
Patient problems
- No Consequences Or Impact To Patient1
- No Information1
- Occlusion1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 7, 2020Infusion or Flow Problem; Infusion or Flow Problem
IT WAS REPORTED TO VYAIRE MEDICAL THAT OUR CK0010 NEB KIT W ADAPTER STERILE WATER 1000ML WAS NOT MISTING. THE RESPIRATORY THERAPIST SUGGESTED THAT THE LONG STEM ON THE ADAPTOR KITS WAS NOT ALLOWING THE MIST TO FORM. AT THIS TIME, THERE WAS NO INFORMATION ON PATIENT INVOLVEMENT IN THIS REPORTED EVENT.
Patient problems: No Information
MAUDE report 10382896 ↗InjuryJan 10, 2020Infusion or Flow Problem; Infusion or Flow Problem
THE CUSTOMER REPORTED THAT DURING USE ON PATIENT THEIR NEBULIZER KIT'S MISTS WORKS FINE INITIALLY BUT WHEN THEY TURN OFF THE FLOW AND RESTARTED IT AGAIN IT DOES NOT WORK ANYMORE. NO PATIENT HARM WAS REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9578747 ↗InjuryJan 10, 2020Infusion or Flow Problem; Infusion or Flow Problem
THE CUSTOMER REPORTED THAT THE PATIENT'S AEROSOL HUMIDIFIER OF CC10 CAP NEBULIZER 24 PACK HAS STOPPED PRODUCING MIST EVEN THOUGH THE BOTTLE HAD WATER IN IT AND THE FLOW WAS ADEQUATE. PATIENT STOPPED RECEIVING HUMIDITY RESULTING IN MUCUS PLUGGING. EMERGENCY TRACHEOSTOMY CHANGE WAS DONE AND THE EQUIPMENT WAS REMOVED FROM THE PATIENT. PATIENT HARM IS NOT KNOWN AT THIS TIME.
Patient problems: Occlusion
MAUDE report 9575549 ↗
Other NEBULIZER (DIRECT PATIENT INTERFACE) devices
- HUDSON RCI IPN049807Teleflex Incorporated · NEBULIZER (DIRECT PATIENT INTERFACE)62 reports
- Circulaire™ 0330Sunmed, LLC · Nebulizer (Direct Patient Interface)1 recall0 reports
- I neb 00Respironics Respiratory Drug Delivery (Uk) Ltd · NEBULIZER (DIRECT PATIENT INTERFACE)3 deaths15 reports
- VixOne 0209Westmed, Inc. · Nebulizer (Direct Patient Interface)13 reports
- HUDSON RCI IPN040620Teleflex Incorporated · NEBULIZER (DIRECT PATIENT INTERFACE)12 reports
- HUDSON RCI HUD05014Medline Industries, Inc. · Nebulizer (direct patient interface)6 reports
- HUDSON RCI IPN049808Teleflex Incorporated · NEBULIZER (DIRECT PATIENT INTERFACE)6 reports
- VixOne 0210Westmed, Inc. · Nebulizer (Direct Patient Interface)5 reports
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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