Drive R726GRRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00822383233215), received between Aug 12, 2020 and Apr 13, 2022 — classified as 2 injuries.

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. How this data works · Data updated Oct 13, 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.

• InjuryApr 13, 2022Break; Break

  (B)(6) HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR ON (B)(6) 2021, BUT DID NOT RECEIVE SPECIFIC INFORMATION REGARDING THE INJURY UNTIL ON (B)(6) 2022. THE END USER WAS REPORTEDLY SITTING ON THE UNIT WHEN THE BACKREST BROKE, CAUSING HIM TO FALL AND FRACTURE A RIB. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO INSPECT THE PRODUCT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Bone Fracture(s); Fall

  MAUDE report 14105269 ↗
• InjuryAug 12, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A ROLLATOR. THE DEVICE HAS NOT BEEN RETRIEVED FOR INVESTIGATION. END-USER WAS DESCENDING FROM THE CAR REACHING OUT FOR THE ROLLATOR WHEN SHE CUT HER LEG ON THE BRAKES. SHE WAS TAKEN TO THE HOSPITAL BY AMBULANCE WHERE SHE RECEIVED STITCHES. THEY WERE UNABLE TO REATTACH ALL THE SKIN AFFECTED. CUSTOMER HAVE BEEN TOLD IN THE HOSPITAL THAT IT COULD TAKE AS LONG AS A YEAR TO HEAL. CUSTOMER IS CURRENTLY ON HOME HEALTH CARE FOR THIS INJURY.

  Patient problems: Laceration(s)

  MAUDE report 10396976 ↗