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PLR975MRecalls & 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
3
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00606509400930), received between Oct 12, 2020 and Jun 24, 2025 — classified as 1 injury, 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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 1 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Appropriate Device Problem Term/Code Not Available3

Patient problems

  • No Clinical Signs, Symptoms or Conditions2
  • Abrasion1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 24, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    PROVIDER ALLEGES THEIR CUSTOMER WAS LOWERING THEIR CHAIR WHEN THE TRANSFORMER/MOTOR CABLE WAS SMASHED AND IT ALLEGEDLY CAUSED A SMALL FIRE AND BURNED THEIR RUG.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22320241 ↗
  • InjuryJan 12, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    IDER ALLEGES CONSUMER ALLEGES FABRIC IS BLEEDING ONTO HIS CLOTHES AND SKIN ALLEGEDLY CAUSING HIM TO GET A RASH.

    Patient problems: Abrasion

    MAUDE report 16148076 ↗
  • MalfunctionOct 12, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    ALLEGES BASE MOTOR IS BARELY WORKING AND SOUNDS LIKE SOMETHING INSIDE THE BOX IS GRINDING. ALLEGES HAD TO CALL THE FIRE DEPARTMENT TO GET USER OUT OF THE CHAIR.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10661037 ↗

Other Chair, Positioning, Electric devices

All Chair, Positioning, Electric devices →

Sources and updates

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