Medline RTACIACMRecalls & reported problems
Medline Industries, Inc. · REGULATOR,SUCTION,CONT/INT,NO BTM,CHEM · Class 2
- 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 10193489014235), received between Sep 9, 2026 and Sep 9, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Suction Failure” (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
- Suction Failure1
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.
MalfunctionSep 9, 2026Suction Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50694643 ↗
Other REGULATOR, VACUUM devices
- Ohio Medical Vacuum Regulator PISAOhio Medical, LLC · Regulator, Vacuum1 recall2 reports
- Medline RTACIBOMMedline Industries, Inc. · REGULATOR, VACUUM7 reports
- Medline RTACIDCMMedline Industries, Inc. · REGULATOR, VACUUM6 reports
- Medline RTACIAAAMedline Industries, Inc. · REGULATOR, VACUUM5 reports
- Medline RTACIVCMMedline Industries, Inc. · REGULATOR, VACUUM2 reports
- Medline RTACIBCMMedline Industries, Inc. · REGULATOR, VACUUM2 reports
- Medline RTACIBOMYMedline Industries, Inc. · REGULATOR, VACUUM2 reports
- Medline RTAC3BPBMedline Industries, Inc. · REGULATOR, VACUUM1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.