Precision Medical Blender PM5200Recalls & reported problems
Precision Medical, Inc. · PM5200 SERIES,BLENDER,AIR/O2,HIGH FLOW · 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 00855887006009), received between Jan 5, 2017 and Jan 5, 2017.
The most frequently reported specific device problem is “Free or Unrestricted Flow” (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
- Free or Unrestricted Flow1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
Jan 5, 2017Free or Unrestricted Flow
PT FOUND ON HIGH FLOW NASAL CANNULA EQUIPMENT OVER FLOWING WITH WATER ENTERING TUBING ATTACHED TO PATIENT AND RUSHING INTO PATIENT NOSE . IMMEDIATELY DISCONNECTED PATIENT FROM MACHINE .
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6224811 ↗
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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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