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Drive KA2200S-2GWPRecalls & reported problems

Drive Devilbiss Healthcare · Nimbo with Seat, S, Wizard Purple · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383583983), received between Dec 16, 2022 and Dec 16, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Failure to Align” (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

Device problems

  • Failure to Align1

Patient problems

  • Bruise/Contusion1
  • Fall1
  • Swelling/ Edema1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryDec 16, 2022Failure to Align; Failure to Align

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A POSTERIOR WALKER BY AN END USER, WHO STATED THAT THE WHEELS TO HER WALKER BECAME CAUGHT IN A DOORWAY, CAUSING HER TO FALL TO THE GROUND AND SUSTAIN BRUISING, SWELLING, AND BLEEDING TO HER FACE. THE END USER CONSULTED A DOCTOR AFTER THE INCIDENT TO CONFIRM THAT THERE WAS NO FURTHER INJURY. 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; Swelling/ Edema

    MAUDE report 15995416 ↗

Other WALKER, MECHANICAL devices

All WALKER, MECHANICAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.