DRIVEMEDICAL 10890Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383123882), received between Oct 10, 2022 and Oct 10, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Temperature Problem” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryOct 10, 2022Temperature Problem; Temperature Problem

  (B)(6) HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A HEATING PAD BY AN END USER, WHO STATED THAT "SHE WAS SLEEPING WHEN THE FUSE BLEW AND BURNED ON HER LOWER BACK." SHE DID NOT SEEK MEDICAL CARE, AND TREATED THE BURN WITH NEOSPORIN. THE END USER DID NOT SPECIFY WHETHER SHE WAS LYING ON THE HEATING PAD WHEN THE INCIDENT OCCURRED, IN CONTRAVENTION OF WARNINGS. ALTHOUGH A REPLACEMENT WAS PROVIDED, ALONG WITH A FREE MAILING LABEL TO RETURN THE AFFECTED UNIT, THE UNIT WAS NEVER RETURNED FOR EVALUATION.

  Patient problems: Superficial (First Degree) Burn

  MAUDE report 15573665 ↗