V. Mueller MO141Recalls & reported problems
Steris Corporation · V. Mueller MCIVOR MOUTH GAG FRAME ONLY · 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 10885403058066), received between Nov 22, 2023 and Nov 22, 2023 — classified as 1 malfunction.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Burn(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 22, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE USER FACILITY REPORTED THAT A PATIENT RECEIVED A "BURN" ON THEIR LIP FROM THE MCIVOR MOUTH GAG. CREAM WAS ADMINISTERED TO THE PATIENT'S LIP AND NO ADDITIONAL MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.
Patient problems: Burn(s)
MAUDE report 18190131 ↗
Other GAG, MOUTH devices
- MicroFrance® MCL206Integra Microfrance · GAG, MOUTH1 report
- AESCULAP OM048RAesculap AG · GAG, MOUTH1 report
- MicroFrance® 7803S-2Integra Microfrance · GAG, MOUTH1 report
- Integra® Jarit® 450110RIIntegra Lifesciences Production Corporation · GAG, MOUTH1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.