LC525iLRecalls & 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 00606509400091), received between Oct 30, 2018 and Oct 26, 2021 — 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.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available6
- No Apparent Adverse Event1
Patient problems
- Bruise/Contusion2
- No Clinical Signs, Symptoms or Conditions2
- Bone Fracture(s)1
- Hip Fracture1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryOct 26, 2021No Apparent Adverse Event; Appropriate Device Problem Term/Code Not Available; No Apparent Adverse Event; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES WHEN GOING INTO A RECLINE POSITION THE BACK ALLEGEDLY BROKE IN HALF AND SHE ALLEGEDLY FELL BACKWARDS WITH A QUICK JOLT.
Patient problems: Bruise/Contusion; No Clinical Signs, Symptoms or Conditions
MAUDE report 12698813 ↗MalfunctionOct 12, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S WIFE ALLEGES WHILE IN THE RECLINE POSITION, THE CONTROLLER QUIT WORKING. CONSUMER'S WIFE AND SON TRIED TO GET THE CONSUMER OUT OF THE CHAIR MANUALLY. THE CONSUMER COULD NOT GET HIS FOOTING, AND ALLEGEDLY SLID TO THE GROUND.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10661048 ↗InjuryMar 18, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER IS ALLEGING HER HUSBAND FELL OUT OF HIS LIFT CHAIR. CLAIMING THE VINYL FABRIC ON THE CHAIR IS CAUSING CONSUMER TO FALL OUT OF CHAIR.
Patient problems: Bruise/Contusion
MAUDE report 9847449 ↗MalfunctionJan 9, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CHAIR WAS STUCK IN THE RECLINE POSITION AND THE CONSUMER ALLEGEDLY CALLED EMT'S TO GET HIM OUT OF THE CHAIR.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9569634 ↗InjuryDec 10, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES HAND CONTROL BUTTON STUCK AND CHAIR DUMPED CUSTOMER OUT WHEN LIFTING.
Patient problems: Hip Fracture
MAUDE report 9446028 ↗InjuryOct 30, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
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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