Walgreens 369353Recalls & reported problems
Walgreen CO. · Toilet Safety Rail. Supports up to 300 lb (136 kg). · Class 1
All models of Walgreens (38)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00311917171319), received between Nov 28, 2018 and Nov 28, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Material Twisted/Bent” (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 16, 2026.
Most reported problems
Device problems
- Material Twisted/Bent1
Patient problems
- Bone Fracture(s)1
- Bruise/Contusion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 28, 2018Material Twisted/Bent
IT WAS REPORTED THAT THE ARM BENT ON THE TOILET SAFETY RAIL AND THE CUSTOMER FELL.
Patient problems: Bone Fracture(s); Bruise/Contusion
MAUDE report 8110833 ↗
Other Adaptor, Hygiene devices
- DRIVEMEDICAL RTL12505Drive Devilbiss Healthcare · ADAPTOR, HYGIENE19 reports
- Drive RTL12202KDRDrive Devilbiss Healthcare · ADAPTOR, HYGIENE11 reports
- Drive 12011KD-1Drive Devilbiss Healthcare · ADAPTOR, HYGIENE1 death9 reports
- Drive RTL12203KDRDrive Devilbiss Healthcare · ADAPTOR, HYGIENE9 reports
- DRIVEMEDICAL 12486Drive Devilbiss Healthcare · ADAPTOR, HYGIENE6 reports
- DMI 522-1702-1900D-M-S Holdings, Inc. · Adaptor, Hygiene5 reports
- DRIVEMEDICAL RTL12027RADrive Devilbiss Healthcare · ADAPTOR, HYGIENE4 reports
- Drive 11135-1Drive Devilbiss Healthcare · ADAPTOR, HYGIENE4 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page