Precision Medical Inc. PM3600 SERIESRecalls & reported problems
Precision Medical, Inc. · PM3600 SERIES,VAC REG,CONT,3POSN,760MMHG · Class 2
Data updated Oct 18, 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 00855887006269), received between Sep 12, 2022 and Sep 12, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Overheating of Device” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Overheating of Device1
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 12, 2022Overheating of Device; Overheating of Device
IT WAS REPORTED THAT, THE HANDLE OF THE MOTOR DRIVE UNIT GOT HOT. NO CASE REPORTED; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15405951 ↗
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- Medline RTACIBOMMedline Industries, Inc. · REGULATOR, VACUUM7 reports
- Medline RTACIDCMMedline Industries, Inc. · REGULATOR, VACUUM6 reports
- Medline RTACIAAAMedline Industries, Inc. · REGULATOR, VACUUM5 reports
- Medline RTACIBCMMedline Industries, Inc. · REGULATOR, VACUUM2 reports
- Medline RTACIVCMMedline Industries, Inc. · REGULATOR, VACUUM2 reports
- Medline RTACIBOMYMedline Industries, Inc. · REGULATOR, VACUUM2 reports
- Amvex Vacuum Regulator PIDOhio Medical, LLC · 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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