Medisorb™ 2079796-001Recalls & reported problems
AirLife Finland Oy · Medisorb™ EX, Disposable · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10889483577417), received between Aug 1, 2025 and Aug 29, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “No Flow” (2 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.
Reports received per month
Most reported problems
Device problems
- No Flow2
- No Pressure2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 29, 2026No Flow; No Pressure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50509923 ↗MalfunctionAug 1, 2025No Flow; No Pressure; No Flow; No Pressure
IT WAS REPORTED THAT THERE WAS AN ANESTHETIC MACHINE FAULT. THE CIRCUIT WOULD NOT PRESSURIZE. IT IS UNKNOWN IF THERE WAS PATIENT INJURY, HARM OR DELAY IN THERAPY, ALTHOUGH, IF THIS MALFUNCTION WERE TO RECUR DURING PATIENT USE THERE IS A POSSIBILITY OF DELAY IN TREATMENT, SERIOUS INJURY OR HARM TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22692402 ↗
Other Absorbent, Carbon-Dioxide devices
- Medisorb™ M1173310AirLife Finland Oy · ABSORBENT, CARBON-DIOXIDE8 reports
- Medisorb™ M1173311AirLife Finland Oy · ABSORBENT, CARBON-DIOXIDE3 reports
- AMSORB® PLUS AMAB3801GEArmstrong Medical Ltd · Absorbent, Carbon-Dioxide3 reports
- PC 55-01-0017Allied Medical, LLC · Absorbent, Carbon-Dioxide2 reports
- PC 55-01-0027Allied Medical, LLC · Absorbent, Carbon-Dioxide1 report
- MEDLINE DYNJAACO2LFMedline Industries, Inc. · ABSORBENT, CARBON-DIOXIDE1 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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