DRIVEMEDICAL SSP218DFA-SFRecalls & reported problems
Drive Devilbiss Healthcare · Transport/WheelchairWheelchairs K2 Product Description: SlvrSprt2,18"SlvrVeinDetFullArm,ELV,1/cs · Class 1
All models of DRIVEMEDICAL (111)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383268873), received between Jan 24, 2020 and Jan 24, 2020 — classified as 1 death.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Bone Fracture(s)1
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
DeathJan 24, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WHEELCHAIR. THE END-USER'S FAMILY IS IN POSSESSION OF THE WHEELCHAIR. IT IS NOT AVAILABLE FOR EVALUATION. THE END-USER'S FAMILY MEMBER HAS ADVISED THAT THE END-USER WAS BEING TRANSPORTED BY A LOCAL TRANSPORT COMPANY. THE BRAKES OF THE CHAIR WERE NOT LOCKED. THE WHEELCHAIR ROLLED DOWN THE RAMP. THE END-USER FELL AND BROKE HIS FEMUR. HE REPORTEDLY DIED FROM THE FALL. THE TRANSPORT COMPANY IS SUGGESTING THAT THE DEVICE WAS FAULTY. DATE OF DEATH AND MEDICAL INFORMATION IS NOT AVAILABLE DUE TO HIPPA RESTRICTIONS.
Patient problems: Bone Fracture(s); Fall
MAUDE report 9629000 ↗
Other Wheelchair, mechanical devices
- MEDLINE K1186N22SMedline Industries, Inc. · Wheelchair, mechanical48 reports
- Guardian K4186N24EMedline Industries, Inc. · Wheelchair, mechanical22 reports
- MEDLINE INDUSTRIES, INC. MDS808650Medline Industries, Inc. · Wheelchair, mechanical18 reports
- Medline MDS806850Medline Industries, Inc. · Wheelchair, mechanical17 reports
- Quickie 7 SeriesSunrise Medical (US) LLC · Wheelchair, Mechanical1 death10 reports
- Guardian K3186N24EMedline Industries, Inc. · Wheelchair, mechanical10 reports
- Guardian K3206N24SMedline Industries, Inc. · Wheelchair, mechanical9 reports
- MEDLINE K3186N34SMedline Industries, Inc. · Wheelchair, mechanical9 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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