Well at Walgreens 449724Recalls & reported problems
Walgreen CO. · Ultra Light Rollator. Burgundy. Supports up to 250 lbs. · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 1
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00311917124711), received between Apr 23, 2018 and Sep 5, 2023 — classified as 1 death, 5 injuries.
The most frequently reported specific device problem is “Break” (3 reports).
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
Device problems
- Break3
- Appropriate Device Problem Term/Code Not Available1
- Component Falling1
- Detachment Of Device Component1
- Detachment of Device or Device Component1
Patient problems
- Bone Fracture(s)4
- Fall2
- Hip Fracture1
- Joint Dislocation1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
DeathSep 5, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE CUSTOMER ON (B)(6) 2023 HER FATHER "WAS WALKING WITH THE ROLLATOR TO THE BATHROOM AND TURNED THE DEVICE AROUND TO SIT STATIONARY BY THE SINK". PER THE CUSTOMER HER FATHER "SAT DOWN" ON THE STATIONARY DEVICE, BUT WAS UNABLE TO CONFIRM IF THE BRAKES WERE APPLIED WHEN SITTING. PER THE CUSTOMER WHEN HER FATHER SAT DOWN "THE BACK LEFT LEG SNAPPED JUST BELOW THE WELD BY THE CROSS BAR, THROWING THEM BACK AND HITTING THEIR HEAD ON THE BATHROOM TUB".
Patient problems: Bone Fracture(s)
MAUDE report 17683107 ↗InjuryJul 24, 2019Detachment of Device or Device Component
IT WAS REPORTED THAT THE ROLLATOR'S WHEEL CAME OFF WHILE END-USER WAS WALKING USING THE ROLLATOR. THE END-USER FELL AND SUSTAINED RIGHT FEMUR FRACTURE.
Patient problems: Bone Fracture(s)
MAUDE report 8821386 ↗InjuryJul 12, 2019Break
IT WAS REPORTED THAT A ROLLATOR WHEEL BROKE OFF THE DEVICE AND THE END-USER EXPERIENCED A FALL.
Patient problems: Bone Fracture(s); Fall
MAUDE report 8784780 ↗InjuryMar 26, 2019Break
IT WAS REPORTED THAT THE ROLLATOR'S FRONT RIGHT WHEEL BROKE RESULTING IN THE END-USER FALLING AND FRACTURING THE THREE TOES ON THE LEFT FOOT.
Patient problems: Bone Fracture(s)
MAUDE report 8453248 ↗InjuryMay 10, 2018Break; Detachment Of Device Component
IT WAS REPORTED THAT A ROLLATOR WHEEL BROKE OFF AND THE END-USER EXPERIENCED A FALL AND A RIGHT-SIDED SHOULDER DISLOCATION.
Patient problems: Fall; Joint Dislocation
MAUDE report 7502022 ↗InjuryApr 23, 2018Component Falling
WHEEL FELL OFF RESULTING IN THE CUSTOMER FALLING TO THE GROUND WHICH REPORTEDLY RESULTED IN THE CUSTOMER BREAKING HER HIP.
Patient problems: Hip Fracture
MAUDE report 7451139 ↗
Other Walker, Mechanical devices
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- Drive 10257RD-1Drive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- DRIVEMEDICAL 795BDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive R726BKDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive 10215BL-1Drive Devilbiss Healthcare · WALKER, MECHANICAL8 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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