Drive 10226-1Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00822383121680), received between Feb 28, 2019 and Aug 21, 2019 — classified as 2 injuries.

The most frequently reported specific device problem is “Collapse” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryAug 21, 2019Fracture; Fracture

  (B)(4) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WALKER. (B)(4) BECAME AWARE OF THE INCIDENT UPON RECEIPT OF A LAWYER'S LETTER. (B)(4) DOES NOT EXPECT TO RECEIVE THE DEVICE FOR EVALUATION. WE HAVE RECEIVED PHOTOS OF THE BROKEN DEVICE. PATIENT WAS IN THE HOSPITAL RECUPERATING FROM KNEE REPLACEMENT SURGERY. THE HOSPITAL SUPPLIED THE DEVICE TO THE PATIENT. THE WALKER REPORTEDLY BROKE DURING USE CAUSING THE PATIENT TO FALL AND BREAK HIS KNEE CAP. WE ARE AWAITING ADDITIONAL DATA AND SUPPORTING DOCUMENTATION. WE WILL FILE A FOLLOW-UP SUBMISSION IF AND WHEN THIS OCCURS.

  Patient problems: Bone Fracture(s)

  MAUDE report 8918804 ↗
• InjuryFeb 28, 2019Collapse; Collapse

  DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WALKER. THE END-USER GOT OUT OF BED AND WAS USING THE WALKER TO GO TO THE RESTROOM. DURING USE THE WALKER COLLAPSED WHEN ONE OF THE RIVETS IN THE FOLDING MECHANISM GAVE OUT AND ONE OF THE LEGS BENT . THE END-USER FELL INTO A CHEST OF DRAWERS. THE PATIENT SUSTAINED A GASH ON RIGHT LEG, APPROX. 10 INCHES LONG. STITCHES WERE REQUIRED, END USER NOT SURE HOW MANY WERE NEEDED.

  Patient problems: Fall; Laceration(s)

  MAUDE report 8380233 ↗