Medline RTACIVDHRecalls & reported problems
Medline Industries, Inc. · REGULATOR,SUCTION,C/I,NPT TRAP B,DISS HT · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 10193489080551), received between Jun 19, 2026 and Jun 19, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Failure to Power Up” (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
- Failure to Power Up1
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 19, 2026Failure to Power Up
IT WAS REPORTED THAT THE DEVICE WILL NOT POWER ON.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25565876 ↗
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 RTACIACMMedline Industries, Inc. · REGULATOR, VACUUM1 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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