MEDLINE DYNJAACO2LFRecalls & reported problems
Medline Industries, Inc. · ABSORBER,CO2,CANISTER W/ HANDLE, LF · Class 1
- 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 10197344103072), received between Jun 5, 2026 and Jun 5, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Leak/Splash” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Leak/Splash1
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.
MalfunctionJun 5, 2026Leak/Splash
IT WAS REPORTED THAT THE CO2 ABSORBER WAS LEAKING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25418133 ↗
Other ABSORBENT, CARBON-DIOXIDE devices
- Medisorb™ M1173310AirLife Finland Oy · ABSORBENT, CARBON-DIOXIDE8 reports
- AMSORB® PLUS AMAB3801GEArmstrong Medical Ltd · Absorbent, Carbon-Dioxide3 reports
- Medisorb™ M1173311AirLife Finland Oy · ABSORBENT, CARBON-DIOXIDE3 reports
- Medisorb™ 2079796-001AirLife Finland Oy · Absorbent, Carbon-Dioxide2 reports
- PC 55-01-0017Allied Medical, LLC · Absorbent, Carbon-Dioxide2 reports
- PC 55-01-0027Allied Medical, LLC · Absorbent, Carbon-Dioxide1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.