WarmTouch 5030850Recalls & reported problems
Covidien LP · Pediatric Surgical Blanket · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20884521061511), received between Jun 19, 2024 and Jul 16, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Patient Device Interaction Problem2
Patient problems
- Burn(s)2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 16, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
ACCORDING TO THE REPORTER, DURING USE, THE PEDIATRIC BLANKET CAUSED FIRST DEGREE BURNS TO THE PATIENT.
Patient problems: Burn(s)
MAUDE report 19756282 ↗MalfunctionJun 19, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
ACCORDING TO THE REPORTER, DURING USE, A PEDIATRIC BLANKET CAUSED BURNS TO THE PATIENT.
Patient problems: Burn(s)
MAUDE report 19571097 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.