DRIVEMEDICAL TITANAXS-BASERecalls & reported problems
Drive Devilbiss Healthcare · PowerMid Wheel Product Description: Titan AXS K0823 MWD Base Only · Class 2
All models of DRIVEMEDICAL (111)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00822383933924), received between Feb 3, 2023 and Jul 25, 2023 — classified as 3 injuries, 1 malfunction.
The most frequently reported specific device problem is “Unintended Collision” (2 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
- Unintended Collision2
- Misassembled During Installation1
- Sharp Edges1
Patient problems
- Bruise/Contusion2
- Laceration(s)1
- Wound Infection1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryJul 25, 2023Misassembled During Installation; Misassembled During Installation
DEVILBISS HEALTHCARE WAS NOTIFIED THROUGH CLAIMS OF A COMPLAINT INVOLVING A POWERED WHEELCHAIR. THE END USER'S ATTORNEY STATED THAT THE "FOOTREST BECAME LOOSE AND [THE END USER] SUFFERED A CUT ON HIS TOE FROM THE SCREW WHICH LED TO AN INFECTION AND SUBSEQUENTLY THAT TOE HAD TO BE AMPUTATED." THERE WERE NO ADDITIONAL DETAILS AS TO WHAT TYPE OF MEDICAL TREATMENT WAS SOUGHT WITHIN THE INITIAL COMPLAINT. 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: Wound Infection
MAUDE report 17386555 ↗InjuryJun 15, 2023Sharp Edges; Sharp Edges
DEVILBISS HEALTHCARE WAS NOTIFIED THROUGH CLAIMS OF A COMPLAINT INVOLVING A POWERED WHEELCHAIR. THE END USER'S ATTORNEY STATED THAT THE "FOOTREST BECAME LOOSE AND [THE END USER] SUFFERED A CUT ON HIS TOE FROM THE SCREW WHICH LED TO AN INFECTION AND SUBSEQUENTLY THAT TOE HAD TO BE AMPUTATED." THERE WERE NO ADDITIONAL DETAILS AS TO WHAT TYPE OF MEDICAL TREATMENT WAS SOUGHT WITHIN THE INITIAL COMPLAINT. 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: Laceration(s)
MAUDE report 17139739 ↗InjuryApr 26, 2023Unintended Collision; Unintended Collision
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A POWERCHAIR BY AN END USER, WHO STATED THAT "WHILE DRIVING FORWARD, THE SPEED INCREASED DRASTICALLY AND THE CHAIR GOT RAMMED INTO HER HOSPITAL BED, BANGING HER LEG INTO THE METAL FRAME," CAUSING A "LARGE LUMP" STICKING OUT OF HER LEFT LEG. THE END USER WENT TO THE HOSPITAL, WHERE IT WAS DETERMINED THAT NOTHING WAS BROKEN. 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: Bruise/Contusion
MAUDE report 16821001 ↗MalfunctionFeb 3, 2023Unintended Collision; Unintended Collision
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A POWERCHAIR BY AN END USER, WHO STATED THAT "WHILE DRIVING FORWARD, THE SPEED INCREASED DRASTICALLY AND THE CHAIR GOT RAMMED INTO HER HOSPITAL BED, BANGING HER LEG INTO THE METAL FRAME," CAUSING A "LARGE LUMP" STICKING OUT OF HER LEFT LEG. THE END USER WENT TO THE HOSPITAL, WHERE IT WAS DETERMINED THAT NOTHING WAS BROKEN. 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: Bruise/Contusion
MAUDE report 16294218 ↗
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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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