PC 55-01-0027Recalls & reported problems
Allied Medical, LLC · CARBOLIME,GEMULTISTYLE,6/CS · 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 00026072025321), received between Nov 14, 2025 and Nov 14, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Gas/Air Leak” (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
- Gas/Air Leak1
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.
MalfunctionNov 14, 2025Gas/Air Leak; Gas/Air Leak
CUSTOMER HAS REPORTED LEAK TEST, FAILURES, ISSUES REQUIRING INTERVENTION MID CASE AT LEAST ONCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23560517 ↗
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
- MEDLINE DYNJAACO2LFMedline Industries, Inc. · ABSORBENT, CARBON-DIOXIDE1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.