Hot Dog Chest and Torso Warming Blanket B110Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00855913001480), received between Jan 22, 2025 and Jan 22, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Degraded” (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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJan 22, 2025Degraded; Use of Device Problem; Degraded; Use of Device Problem

  AS DESCRIBED BY THE REPORTER IN THE AUGUSTINE TEMPERATURE MANAGEMENT'S INCIDENT REPORT FORM "GENERAL ANESTHESIA DENTISTRY. PATIENT WAS PREPPED IN THE PRE-OP, BROUGHT INTO THE OR, PLACED ON THE OR BED. ANESTHESIA BEGAN MASKING DOWN/INTUBATION. AFTER INTUBATION THE PATIENT WAS COVERED BY A BLANKET, THEN THE [HOTDOG] WARMING BLANKET. A STRAP WAS PLACED GENTLY OVER THE PATIENT TO SECURE THEM TO THE OR TABLE AND SURGERY BEGAN. ONCE SURGERY WAS COMPLETED, THE [HOTDOG] WAS REMOVED AND THE BLANKET WAS PUT ONTO THE TRANSFERRING GURNEY. PATIENT WAS TRANSFERRED TO PACU. PACU TEAM SAW THE SKIN AND ASSESSED WITHIN THEIR LIMITS." THE REPORTER MENTIONED [AFTER THE PROCEDURE] "BLISTERS AND RED SKIN IN AREAS. WE WERE NOT ABLE TO DIAGNOSE DEGREE OF BURN ON SITE." THE SIZE AND THE DEGREE OF THE BURN ARE NOT MENTIONED. THE REPORTER SENT IMAGES. THE REPORTER ALSO WROTE: "PATIENT WENT TO URGENT CARE TO GET AREA ASSESSED. PRESCRIBED BURN OINTMENT." PER AUGUSTINE'S INVESTIGATION: WE WERE NOTIFIED IN APR 2024 VIA AN EMAIL ABOUT AN INJURY OCCURRING ON JAN 2024. THE CUSTOMER SENT US A PARTIALLY FILLED OUT INCIDENT REPORT THAT DESCRIBED AN INJURY ON A PEDIATRIC PATIENT, WHERE OUR WARMING DEVICE WAS INVOLVED.

  Patient problems: Partial thickness (Second Degree) Burn

  MAUDE report 21213456 ↗
• InjuryJan 22, 2025Degraded; Use of Device Problem; Degraded; Use of Device Problem

  AS DESCRIBED BY THE REPORTER IN THE AUGUSTINE TEMPERATURE MANAGEMENT'S INCIDENT REPORT FORM "GENERAL ANESTHESIA DENTISTRY. PATIENT WAS PREPPED IN THE PRE OP, BROUGHT INTO THE OR, PLACED ON THE OR BED. ANESTHESIA BEGAN MASKING DOWN/INTUBATION. AFTER INTUBATION THE PATIENT WAS COVERED BY A BLANKET, THEN THE [HOTDOG] WARMING BLANKET. A STRAP WAS PLACED GENTLY OVER THE PATIENT TO SECURE THEM TO THE OR TABLE AND SURGERY BEGAN. ONCE SURGERY WAS COMPLETED, THE [HOTDOG] WAS REMOVED AND THE BLANKET WAS PUT ONTO THE TRANSFERRING GURNEY. PATIENT WAS TRANSFERRED TO PACU. PACU TEAM SAW THE SKIN AND ASSESSED WITHIN THEIR LIMITS." THE REPORTER MENTIONED [AFTER THE PROCEDURE] "BLISTERS AND RED SKIN IN AREAS. WE WERE NOT ABLE TO DIAGNOSE DEGREE OF BURN ON SITE." THE SIZE AND THE DEGREE OF THE BURN ARE NOT MENTIONED. THE REPORTER SENT IMAGES. THE REPORTER ALSO WROTE: "PATIENT WENT TO URGENT CARE TO GET AREA ASSESSED. PRESCRIBED BURN OINTMENT." PER AUGUSTINE'S INVESTIGATION: WE WERE NOT NOTIFIED BY THE MEDICAL FACILITY ABOUT THIS SITUATION WHEN THE EVENT OCCURRED. WE LEARNED ABOUT THIS ADVERSE EVENT FILED BY THE HOSPITAL, VIA A MEDWATCH REPORT SENT TO US BY THE FDA (MW5151770). THE MEDWATCH REPORT RE

  Patient problems: Partial thickness (Second Degree) Burn

  MAUDE report 21213440 ↗