LC250Recalls & 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 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 00606509400237), received between Jun 5, 2018 and Oct 30, 2025 — classified as 4 injuries, 8 malfunctions.
The most frequently reported specific device problem is “Fire” (1 report).
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available11
- Fire1
- Smoking1
- Sparking1
Patient problems
- No Clinical Signs, Symptoms or Conditions7
- Burn(s)2
- Bruise/Contusion1
- No Known Impact Or Consequence To Patient1
- Superficial (First Degree) Burn1
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 30, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
THE CARE GIVER ALLEGES THE REMOTE ALLEGEDLY CAUGHT FIRE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23424401 ↗MalfunctionJul 15, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
INSURANCE COMPANY ALLEGES A FIRE OCCURRED WHERE A PRIDE LIFT CHAIR WAS PRESENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22511509 ↗InjuryMay 2, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
THE PROVIDER ALLEGES THAT THE HAND CONTROL ALLEGEDLY CAUGHT ON FIRE AND SLIGHTLY BURNED THE CUSTOMER.
Patient problems: Burn(s)
MAUDE report 21949348 ↗MalfunctionMar 6, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THE HAND CONTROL CAUGHT ON FIRE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18848276 ↗InjuryJan 18, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CHAIR IS SLOPED TO THE RIGHT ALLEGEDLY CAUSING PRESSURE SORES.
Patient problems: Bruise/Contusion
MAUDE report 18533852 ↗InjuryNov 16, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER ALLEGES HAND CONTROL CAUGHT ON FIRE AND ALLEGEDLY BURNED THEIR HAND.
Patient problems: Burn(s)
MAUDE report 15805564 ↗MalfunctionApr 28, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES SHE WAS USING THE HAND CONTROL ON HER LIFT CHAIR WHEN SHE ALLEGEDLY HER A POP AND ALLEGEDLY A FLAME CAME FROM THE HAND CONTROL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14235868 ↗MalfunctionDec 13, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES, CONSUMER ALLEGES, THE CORD ALLEGEDLY CAUGHT ON FIRE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12983291 ↗InjuryAug 2, 2021Fire; Smoking; Sparking; Fire; Smoking; Sparking
ALLEGES THE HAND CONTROL CAUGHT FIRE. ALLEGES SHE WAS PUSHING THE BUTTONS TO GET OUT OF THE CHAIR WHEN IT STARTED SMOKING AND SPARKING, THEN CAUGHT FIRE.
Patient problems: Superficial (First Degree) Burn
MAUDE report 12259143 ↗MalfunctionMay 17, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES RAISING THE CHAIR TO EXIT AND THE UNIT FLIPPED ON TOP OF CONSUMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11831012 ↗MalfunctionMay 17, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER HAD THEIR CHAIR PLUGGED INTO A POWER STRIP WITH OTHER CONNECTIONS AND THE STRIP ALLEGEDLY CREATED A LITTLE FIRE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11831010 ↗MalfunctionJun 5, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES ONE SIDE OF CHAIR DROPPED AND CUSTOMER FELL OUT OF THE UNIT. PARAMEDICS WERE CALLED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7568319 ↗
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
- LC358L LC358L/CA358LPride Mobility Products Corp · Chair, Positioning, Electric21 reports
- LC358XXL LC358XXL/CA358XXLPride Mobility Products Corp · Chair, Positioning, Electric21 reports
- LC358XL LC358XL/CA358XLPride Mobility Products Corp · Chair, Positioning, Electric18 reports
- LC358M LC358M/BC358M/CA358MPride Mobility Products Corp · Chair, Positioning, Electric1 death11 reports
- LC358PW LC358PW/CA358PWPride Mobility Products Corp · Chair, Positioning, Electric7 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 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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