LC358PW LC358PW/CA358PWRecalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00606509400275), received between Nov 20, 2018 and Jun 21, 2026 — classified as 2 injuries, 5 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjuryJun 21, 2026Appropriate Device Problem Term/Code Not Available

  PROVIDER ALLEGES CONSUMER ALLEGES THE HAND CONTROL SPARKED, BEGAN TO SMOKE, AND ALLEGEDLY A SMALL FLAME APPEARED. CONSUMER IMMEDIATELY THREW THE HAND CONTROL TO THE GROUND ALLEGEDLY SUSTAINING A BURN IN THE PROCESS. CONSUMER ALSO ALLEGES THAT BLACK SMOKE RESIDUE IS VISIBLE ON HER WALL.

  Patient problems: Burn(s)

  MAUDE report 25572219 ↗
• MalfunctionOct 2, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  PROVIDER ALLEGES WIRES WERE EXPOSED FROM WEAR AND TEAR AND WIRES GROUNDED/TOUCHED AND SPARKED AND CAUGHT ON FIRE AND THEN SHUT OFF.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23199169 ↗
• MalfunctionApr 28, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  CONSUMER ALLEGES SHE WAS IN THE CHAIR AND ALLEGEDLY GOT A LITTLE SHOCK, HER CHAIR ALLEGEDLY STARTED MOVING ON ITS OWN AND THERE WERE NO LIGHTS SHOWING ON THE HAND CONTROLLER. SHE SAID THEN THE HAND CONTROL ALLEGEDLY STARTED SMOKING AND ALLEGEDLY CAUGHT FIRE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16830868 ↗
• MalfunctionNov 30, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  CONSUMER ALLEGES THE HAND CONTROL SHOCKED HER AND ALLEGEDLY CAUGHT ON FIRE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15886931 ↗
• MalfunctionFeb 1, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  CONSUMER ALLEGES THE UNIT GOT STUCK IN THE RECLINE POSITION AND THE CONSUMER ALLEGEDLY CALLED 911 TO GET THEM OUT OF THE CHAIR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13417413 ↗
• InjuryJan 25, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  CONSUMER'S DAUGHTER ALLEGES THERE IS NO STUFFING IN THE SEAT AND YOU CAN FEEL THE WOOD WHICH IS ALLEGEDLY GIVING HER MOM SORES.

  Patient problems: Pressure Sore/Ulcer

  MAUDE report 11223842 ↗
• MalfunctionNov 20, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  CONSUMER ALLEGES THAT THEY HAVE HAS SEVERAL ISSUES WITH LIFT CHAIR AND ON 3 DIFFERENT OCCASIONS THEY NEEDED TO CALL THE PARAMEDICS TO HELP THEM GET OUT OF THE CHAIR.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8090908 ↗