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Walgreens 276741Recalls & reported problems

Walgreen CO. · Walgreens Folding Paddle Walker with 5" Wheels. Fits most adults 5 ft- 6 ft 3 in. Supports up to 350 lb. · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00311917158938), received between Jan 9, 2020 and Feb 13, 2020 — classified as 1 injury, 1 malfunction.

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

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Break1
  • Collapse1

Patient problems

  • Bone Fracture(s)1
  • Bruise/Contusion1
  • Fall1
  • Pain1
  • Vertigo1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryFeb 13, 2020Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT WHILE WALKING UP A HANDICAP ACCESS RAMP WITH A ROLLATOR, THE RIGHT HANDLE OF THE ROLLATOR "FLEW-OUT" TO THE RIGHT RESULTING IN THE END-USER EXPERIENCING A FALL TO THE GROUND AND A SCAPHOID FRACTURE.

    Patient problems: Bone Fracture(s)

    MAUDE report 9707646 ↗
  • MalfunctionJan 9, 2020Break; Collapse

    IT WAS REPORTED THAT THE RIGHT-SIDED HANDLE OF THE WALKER BROKE, THE DEVICE "COLLAPSED," AND THE END-USER EXPERIENCED A FALL.

    Patient problems: Bruise/Contusion; Fall; Pain; Vertigo

    MAUDE report 9568790 ↗

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.