DRIVEMEDICAL 10220-1WWRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00822383901145), received between May 26, 2020 and Jun 20, 2023 — 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. 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 20, 2023Break; Break

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF A COMPLAINT REGARDING A WALKER BY AN END USER, WHO STATED THAT "THE [HANDLE] BAR BROKE ON BOTH ENDS AND SHEARED OFF " AND SHE REPORTEDLY FELL AND SUSTAINED BRUISING. THE END USER REPORTED THAT SHE HAS HOME HEALTH AIDES TO TEND TO HER BRUISING AND SHE WILL BE SCHEDULING AN X-RAY. 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: Bruise/Contusion; Fall

  MAUDE report 17167329 ↗
• InjuryMay 26, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DRIVE DEVILBISS IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WALKER. THIS REPORT IS BEING TENDERED IN AN OVERABUNDANCE OF CAUTION IN RESPONSE TO AN MDR REGRESSION ANALYSIS. CUSTOMERS WALKER WAS CAUGHT IN THE CARPET CAUSING HIM TO FALL DAMAGING THE WALKER. HE FELL AND HIT HIS HEAD AND SUSTAINED A SMALL CUT WHICH REQUIRED A STAPLE.

  Patient problems: Fall

  MAUDE report 10090304 ↗