PLR3955MRecalls & reported problems
Pride Mobility Products Corp · An electric positioning chair is a device with a motorized positioning control that is intended for medical purposes and that can be adjusted to various positions. The device is used to provide stability for patients with athetosis (involuntary spasms) and to alter postural positions. · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00606509401494), received between May 8, 2023 and Jul 9, 2026 — classified as 2 injuries, 2 malfunctions.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available3
- No Apparent Adverse Event1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Burn(s)2
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryJul 9, 2026Appropriate Device Problem Term/Code Not Available
ATTORNEY ALLEGES THAT A FIRE OCCURRED AT A PROPERTY WHERE A PRIDE MOBILITY VIVA LIFT POWER RECLINER
Patient problems: Burn(s); No Clinical Signs, Symptoms or Conditions
MAUDE report 25762462 ↗InjuryMay 16, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THE UNIT GETS TOO HOT AND IT ALLEGEDLY BURNS HER. ON 05/07/2025, CONSUMER ALLEGED THAT THE TECH CAME OUT AND SPRAYED THE UNIT WITH WD 40 AND SHE IS ON HER WAY TO THE DOCTOR'S OFFICE. SHE HAS RESPIRATORY ISSUES AND ALLEGEDLY CAN NOT BREATHE.
Patient problems: Burn(s)
MAUDE report 22034771 ↗MalfunctionJun 13, 2024No Apparent Adverse Event; No Apparent Adverse Event
PROVIDER ALLEGES CONSUMER'S TRANSFORMER CAUGHT ON FIRE AND IS SMOKING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19527217 ↗MalfunctionMay 8, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES SHE WAS TRANSPORTING A LIFT CHAIR FROM THE DEALER AND HAD THE BASE OF THE LIFT CHAIR IN THE BED OF HER TRUCK. SHE ALLEGES THE LIFT CHAIR CAUGHT FIRE AND ALLEGEDLY DESTROYED THE CHAIR AND HER TRUCK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16885232 ↗
Other Chair, Positioning, Electric devices
- TruRize 3333Stryker Corporation · Chair, positioning, electric1 recall1 death53 reports
- EasyStand Bantam SmallAltimate Medical Inc. · Chair, Positioning, Electric1 recall0 reports
- EasyStand Bantam Extra SmallAltimate Medical Inc. · Chair, Positioning, Electric1 recall0 reports
- LC358XXL LC358XXL/CA358XXLPride Mobility Products Corp · Chair, Positioning, Electric21 reports
- LC358L LC358L/CA358LPride Mobility Products Corp · Chair, Positioning, Electric21 reports
- LC358XL LC358XL/CA358XLPride Mobility Products Corp · Chair, Positioning, Electric18 reports
- LC250Pride Mobility Products Corp · Chair, Positioning, Electric12 reports
- LC358M LC358M/BC358M/CA358MPride Mobility Products Corp · Chair, Positioning, Electric1 death11 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 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