DRIVEMEDICAL SSP216DDA-SFRecalls & reported problems
Drive Devilbiss Healthcare · Transport/WheelchairWheelchairs K2 Product Description: SlvrSprt2,16"SlvrVeinDetDsk,ElvLg,1/cs · Class 1
All models of DRIVEMEDICAL (111)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00822383145280), received between Jan 31, 2023 and May 12, 2025 — classified as 4 injuries, 1 malfunction.
The most frequently reported specific device problem is “Device Slipped” (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.
Reports received per month
Most reported problems
Device problems
- Device Slipped3
- Use of Device Problem3
- Break1
- Sharp Edges1
Patient problems
- Fall4
- Bone Fracture(s)3
- Loss of consciousness3
- Laceration(s)1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryMay 12, 2025Sharp Edges; Sharp Edges
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WHEELCHAIR BY THE END USER, WHO STATED THAT WHILE MOVING FROM A TOILET SEAT TO THE WHEELCHAIR, A SHARP PROTRUDING PLATE ON THE WHEELCHAIR CAUSED A LACERATION ON THE END USER'S LEFT LEG THAT IS BEING TREATED WITH A SKIN GRAFT. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.
Patient problems: Laceration(s)
MAUDE report 22002277 ↗InjuryOct 23, 2023Device Slipped; Use of Device Problem; Device Slipped; Use of Device Problem
WE RECEIVED THE EMAIL FROM OUR CUSTOMER DRIVE, THE DETAILS AS BELOW: PLEASE FIND ATTACHED A COPY OF THE DRIVE MEDWATCH REPORT # 2438477-2023-00002. THE MEDICAL DEVICE INVOLVED IN THE INCIDENT IS A SLVESPRT2,16IN SLVRVEINDETDSK,SWGFT,1/CS, MODEL NUMBER SSP216DDA-SF. THE SERIAL NUMBER IS (B)(6). PLEASE REFER TO THE MEDWATCH REPORT FOR INFORMATION ABOUT THE EVENT. AS OF TODAY, THE PRODUCT IN QUESTION HAS NOT BEEN RETURNED TO DRIVE MEDICAL FOR EVALUATION. DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WHEELCHAIR BY AN END USER, WHO STATED THAT SHE WAS USING THE WHEELCHAIR "ON THE SIDEWALK UP A RAMP," WHEN IT WAS "RAINING A LOT AND COLD," AND WHERE "THERE WERE A LOT OF LEAVES SO IT WAS SLIPPERY." SHE WAS REPORTEDLY "THROWN OUT OF THE CHAIR" AND WAS RENDERED UNCONSCIOUS. WHEN SHE REGAINED CONSCIOUSNESS, "THE CHAIR WAS ON TOP OF HER," AND SHE SUSTAINED 3 BROKEN RIBS. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
Patient problems: Bone Fracture(s); Fall; Loss of consciousness
MAUDE report 17993197 ↗InjuryJun 2, 2023Break; Break
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF A COMPLAINT REGARDING A WHEELCHAIR BY AN END USER'S MOTHER, WHO STATED THAT HER DAUGHTER "FELL OFF OF HER WHEELCHAIR DUE TO HER WHEEL FALLING OFF WHILE SHE WAS RIDING IT," REPORTEDLY CAUSING HER TO SUSTAIN MINOR SCRAPES, AND LOSS OF A FRONT TOOTH, FOR WHICH SHE RECEIVED PAIN MANAGEMENT IN THE HOSPITAL. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
Patient problems: Fall
MAUDE report 17054443 ↗MalfunctionMay 27, 2023Device Slipped; Use of Device Problem; Device Slipped; Use of Device Problem
ON (B)(6) 2023, WE RECEIVED A EMAIL FROM OUR CUSTOMER DRIVE DEVILBISS HEALTHCARE ABOUT THIS ADVERSE EVENT. THE MEDICAL DEVICE INVOLVED IN THE INCIDENT IS A SLVESPRT2,16IN SLVRVEINDETDSK,SWGFT,1/CS, MODEL NUMBER SSP216DDA-SF. THE SERIAL NUMBER IS (B)(6). DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WHEELCHAIR BY AN END USER, WHO STATED THAT SHE WAS USING THE WHEELCHAIR "ON THE SIDEWALK UP A RAMP," WHEN IT WAS "RAINING A LOT AND COLD," AND WHERE "THERE WERE A LOT OF LEAVES SO IT WAS SLIPPERY." SHE WAS REPORTEDLY "THROWN OUT OF THE CHAIR" AND WAS RENDERED UNCONSCIOUS. WHEN SHE REGAINED CONSCIOUSNESS, "THE CHAIR WAS ON TOP OF HER," AND SHE SUSTAINED 3 BROKEN RIBS. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
Patient problems: Bone Fracture(s); Fall; Loss of consciousness
MAUDE report 17015399 ↗InjuryJan 31, 2023Device Slipped; Use of Device Problem; Device Slipped; Use of Device Problem
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WHEELCHAIR BY AN END USER, WHO STATED THAT SHE WAS USING THE WHEELCHAIR "ON THE SIDEWALK UP A RAMP," WHEN IT WAS "RAINING A LOT AND COLD," AND WHERE "THERE WERE A LOT OF LEAVES SO IT WAS SLIPPERY." SHE WAS REPORTEDLY "THROWN OUT OF THE CHAIR" AND WAS RENDERED UNCONSCIOUS. WHEN SHE REGAINED CONSCIOUSNESS, "THE CHAIR WAS ON TOP OF HER," AND SHE SUSTAINED 3 BROKEN RIBS. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
Patient problems: Bone Fracture(s); Fall; Loss of consciousness
MAUDE report 16274175 ↗
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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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