DRIVEMEDICAL EXP19LTBLRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383259093), received between Sep 27, 2022 and Sep 27, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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 16, 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.

• InjurySep 27, 2022Break; Break

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A TRANSPORT CHAIR BY AN END USER, WHO REPORTED THAT THE "FRAME BROKE," CAUSING HER TO FALL AND SUSTAIN "CUTS ON BOTH ARMS AND ONE SHIN," WHICH DID NOT REQUIRE STITCHES BUT DID REQUIRE "A LOT" OF WOUND CARE. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Fall; Laceration(s)

  MAUDE report 15495513 ↗