Precision Medical Blender PM5300Recalls & reported problems
Precision Medical, Inc. · PM5300 SERIES,BLENDER,AIR/O2,LOW FLOW · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00855887006016), received between Jul 12, 2018 and Mar 2, 2023 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Fire” (2 reports).
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
- Fire2
- Device Damaged by Another Device1
- No Audible Prompt/Feedback1
Patient problems
- Hypoxia1
- No Clinical Signs, Symptoms or Conditions1
- No Patient Involvement1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 2, 2023No Audible Prompt/Feedback; Device Damaged by Another Device; No Audible Prompt/Feedback; Device Damaged by Another Device
NICU RN REPORTED THAT THE BLENDER GAS SUPPLY IMBALANCE ALARM WAS NOT ALARMING PROPERLY AND ADVISED THERE WAS A PATIENT INCIDENT. THE BABY WAS TRANSPORTED TO NICU WITHOUT PROPER OXYGEN RESULTING IN THE BABY BEING HYPOXIC UNTIL ARRIVAL AND STABILIZATION IN NICU. BLENDER WAS TESTED AND THE REPORTED PROBLEM WAS REPRODUCED - REMOVED DEVICE FROM SERVICE. AFTER FURTHER TESTING, AN ADDITIONAL THREE UNITS HAVE BEEN FOUND WITH THE SAME PROBLEM.
Patient problems: Hypoxia
MAUDE report 16469217 ↗InjuryApr 8, 2021Fire; Fire
FIRE INVOLVING PRECISION MEDICAL BLENDER CAUSED BY A HEATING ELEMENT HEAD OF THE WARMER AS DESCRIBED IN THE NARRATIVE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11633153 ↗MalfunctionJul 12, 2018Fire; Fire
FIRE INCIDENT WHICH OCCURRED TO AN OXYGEN BLENDER (5300) IN A NEONATAL INTENSIVE CARE UNIT. THIS INCIDENT WAS REPORTED BY THE HOSPITAL PERSONNEL TO THE (B)(6) AND A COMPLAINT SENT TO US ON (B)(6) 2018. DATE OF ACTUAL OCCURRENCE IS UNKNOWN
Patient problems: No Patient Involvement
MAUDE report 7682122 ↗
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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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