3M™ Bair Hugger™ 67500Recalls & reported problems
3m Company · 3M™ Bair Hugger™ Warming Unit, 67500, 120V-ENG-B, 1 Each · 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 00707387803940), received between Mar 30, 2023 and Mar 30, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fire” (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
- Fire1
- Smoking1
- Sparking1
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.
MalfunctionMar 30, 2023Fire; Smoking; Sparking; Fire; Smoking; Sparking
A CHILDREN'S HOSPITAL ALLEGED AN ELECTRICAL FIRE WITH SPARKING, SMOKING, AND MELTING WITH THE USE OF THE 3M¿ BAIR HUGGER¿ WARMING UNIT, MODEL 675. NO INJURIES AND NO MEDICAL INTERVENTION WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16648262 ↗
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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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