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DMI 522-1702-1900Recalls & reported problems

D-M-S Holdings, Inc. · Chair Shower Transport · Class 1

Adverse event reports
5
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00041298017028), received between Aug 28, 2023 and May 14, 2026 — classified as 1 injury, 4 malfunctions.

The most frequently reported specific device problem is “Unintended Movement” (2 reports).

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: 1 reportsDec 2024: 0 reportsJan 2025: 1 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 1 reportsJun 2025: 0 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: 1 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

  • Unintended Movement2
  • Fracture1
  • Insufficient Device Problem Information1
  • Material Separation1
  • Mechanical Problem1
  • Misassembly by Users1
  • No Apparent Adverse Event1

Patient problems

  • No Clinical Signs, Symptoms or Conditions3
  • Fall1
  • Insufficient Information1

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 14, 2026Fracture; No Apparent Adverse Event

    CLIPS ON ONE SIDE OF SEAT OF UNIT FAILED, CAUSING THE SEAT TO DROP AND USER TO FALL HALFWAY TO THE FLOOR BEFORE SHE CAUGHT HERSELF ON HAND RAILS. NO INJURY TO USER REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25174577 ↗
  • MalfunctionMay 19, 2025Material Separation; Unintended Movement; Material Separation; Unintended Movement

    WHEN THE HOSPICE CAREGIVER PUT PATIENT ON THE SHOWER CHAIR, A CLIP PULLED AWAY FROM THE SEAT REQUIRING CAREGIVERS TO HOLD/SUPPORT PATIENT "IN ORDER" TO KEEPING HIM FROM FALLING TO THE GROUND. NO INJURIES WERE REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22044566 ↗
  • InjuryJan 15, 2025Insufficient Device Problem Information; Insufficient Device Problem Information

    DISTRIBUTOR OF DEVICE REPORTED "HOSPITALIZATION".

    Patient problems: Insufficient Information

    MAUDE report 21163845 ↗
  • MalfunctionNov 14, 2024Unintended Movement; Misassembly by Users; Unintended Movement; Misassembly by Users

    THE PLASTIC TAB ON THE SEAT CHAIR POPPED OFF CAUSING THE SEAT OF THIS CHAIR TO COME OFF AND INDIVIDUAL TO FALL ON THE FLOOR. NO INJURIES WERE REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20684986 ↗
  • MalfunctionAug 28, 2023Mechanical Problem; Mechanical Problem

    WE JUST BOUGHT THIS PRODUCT OFF OF AMAZON FOR MY BROTHER WHO IS CURRENTLY A PARAPLEGIC. HE'S ONLY BEEN USING IT SINCE 6/5 AND YESTERDAY WHEN HE WAS IN THE SHOWER THE CLIP BROKE OFF OF IT AND HE FELL IN THE SHOWER. THE STRUCRAL SOUNDNESS OF THIS PRODUCT IS VERY CONCERNING TO ME. MY BROTHER IS ONLY 140LBS AND DOES NOT REACH THE WEIGHT LIMIT. PLEASE LET ME KNOW AS SOON AS YOU CAN WHAT WE CAN DO TO RESOLVE THIS ISSUE.

    Patient problems: Fall

    MAUDE report 17637593 ↗

Other Adaptor, Hygiene devices

All Adaptor, Hygiene devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.