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