LC525iPWRecalls & 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
- 6
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00606509400114), received between Apr 26, 2018 and Feb 7, 2025 — classified as 4 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 Available6
Patient problems
- Abrasion1
- Injury1
- No Code Available1
- Pain1
- Pressure Sore/Ulcer1
- Sprain1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryFeb 7, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S SON ALLEGES THAT THE LIFT CHAIR SEAT CAUSED SORES ON HIS MOM.
Patient problems: Abrasion
MAUDE report 21332152 ↗MalfunctionNov 7, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES TRYING TO GET UP AND TOOK HAND OFF THE CONTROL FOR THE CHAIR TO STOP AND THE CHAIR DID NOT STOP, KEPT MOVING, AND PUSHED CUSTOMER OUT OF THE CHAIR.
Patient problems: Pain
MAUDE report 9290990 ↗InjuryFeb 1, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THE LUMBAR PILLOW WASN'T WITH THE LIFT CHAIR WHEN IT WAS DELIVERED. CONSUMER ALSO ALLEGES THAT THE MISSING LUMBAR PILLOW CAUSED HER TO GET 3 BED SORES.
Patient problems: Pressure Sore/Ulcer
MAUDE report 8297827 ↗InjuryJul 30, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES CHAIR WENT FROM A RECLINE POSITION ON ITS OWN TO THE HIGHEST POSITION AND DUMPED HIM ON THE FLOOR.
Patient problems: Injury
MAUDE report 7731595 ↗MalfunctionMay 7, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES CUSTOMER GOT STUCK IN LIFTED POSITION AND HAD TO CALL EMS FOR HELP.
Patient problems: No Code Available
MAUDE report 7491172 ↗InjuryApr 26, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES WHEN THE DELIVERY SERVICE SET UP THE CHAIR THEY FAILED TO PUT THE SCREWS ON THAT HOLD THE BACK TOGETHER ALLEGEDLY CAUSING THE CONSUMER TO FALL BACK OUT OF THE CHAIR.
Patient problems: Sprain
MAUDE report 7463966 ↗
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.
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