DRIVEMEDICAL TITAN18CSRecalls & reported problems
Drive Devilbiss Healthcare · PowerPower Front Wheel Product Description: Titan K0821 FWD 18" x 18" Capt.Seat · Class 2
All models of DRIVEMEDICAL (111)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00822383513331), received between Apr 5, 2019 and May 11, 2020 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Device Tipped Over” (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
- Adverse Event Without Identified Device or Use Problem1
- Device Tipped Over1
- Unintended Movement1
Patient problems
- Bone Fracture(s)2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 11, 2020Device Tipped Over; Unintended Movement
(B)(6) HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A POWER CHAIR. THE WHEELS HAD BEEN CATCHING ON CARPET AND UNEVEN TERRAIN CAUSING OCCUPANT TO BE THROWN. THE END-USER WAS GOING DOWN A RAMP BACKWARDS. THE DEVICE FLIPPED FORWARDS. THE END-USER SUSTAINED A BROKEN TIBIA IN HIS LEFT LEG. PRODUCT INCLUDES A SAFETY BELT.
Patient problems: Bone Fracture(s)
MAUDE report 10045791 ↗InjuryApr 5, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
(B)(4) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A POWER CHAIR. THE WHEELS HAD BEEN CATCHING ON CARPET AND UNEVEN TERRAIN CAUSING OCCUPANT TO BE THROWN. THE END-USER WAS GOING DOWN A RAMP BACKWARDS. THE DEVICE FLIPPED FORWARDS. THE END-USER SUSTAINED A BROKEN TIBIA IN HIS LEFT LEG. PRODUCT INCLUDES A SAFETY BELT.
Patient problems: Bone Fracture(s)
MAUDE report 8488536 ↗
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- Permobil M5Permobil, Inc. · Wheelchair, Powered1 recall7 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.
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