Drive 1239RDRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383537580), received between Oct 26, 2023 and Oct 26, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Sharp Edges” (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. How this data works · Data updated Oct 13, 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 26, 2023Sharp Edges; Sharp Edges

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF A COMPLAINT REGARDING A WALKER BY THE END USER, WHO REPORTED THAT SHE "CUT HER LEG OPEN ON THE SCREW FROM THE FOLDING HINGE ON THE FRONT RIGHT ABOVE THE CASTER." THE WOUND WAS TREATED BY A SPECIALIST FOR SKIN GRAFTS. DRIVE DEVILBISS HEALTHCARE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE DEVICE FOR INVESTIGATION. AN UPDATE WILL BE FILED IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Laceration(s)

  MAUDE report 18016169 ↗