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Walgreens 783180Recalls & reported problems

Drive Devilbiss Healthcare · Canes & Crutches Crutches Product Description Walgreens Univ. EZ Adj Crutch 1PR,8PR/CV · 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 00311917203164), received between Aug 21, 2020 and Aug 21, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

Patient problems

  • Fall1
  • Head Injury1

Recent adverse event reports

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

  • InjuryAug 21, 2020Fracture; Fracture

    DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A PAIR OF CRUTCHES. THE END-USER DOES NOT WANT TO RETURN THE DEVICE TO US FOR EVALUATION. WE WILL FILE AN UPDATED REPORT WHEN WE HAVE ADDITIONAL DATA. WHILE IN USE THE BOTTOM HALF OF THE CRUTCH SPLIT IN HALF. THE USER FELL. HE INJURED HIS HEAD, HAS A BLACK EYE, NECK WAS BRUISED. HE WAS TAKEN TO THE HOSPITAL AND WAS IN THE ICU FOR 5 DAYS.

    Patient problems: Fall; Head Injury

    MAUDE report 10440196 ↗

Other CRUTCH devices

All CRUTCH devices →

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