Transcend Chair Series 0731402Recalls & reported problems

Summary

The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00190790004057), received between Feb 13, 2025 and Aug 6, 2026 — classified as 1 injury, 14 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (8 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. 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 15 most recent of 15 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 6, 2026Unintended Movement

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50168261 ↗
• MalfunctionAug 6, 2026Unintended Movement

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50168260 ↗
• MalfunctionMay 14, 2026Unintended Movement

  THE END USER REPORTED WHILE TRANSFERRING A PATIENT DOWN A FLIGHT OF STAIRS, THE PATIENT SHIFTED THEIR WEIGHT AND THE CHAIR BEGAN TO TIP TO THE SIDE. DUE TO THE WEIGHT OF THE PATIENT AND THE CHAIR, THE MEDIC CREW WAS UNABLE TO STOP THE MOVEMENT OF THE CHAIR BUT WERE ABLE TO SLOWLY LOWER THE PATIENT TO THE GROUND WITH THE CHAIR. NO INJURIES WERE REPORTED AS A RESULT OF THE INCIDENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25175353 ↗
• MalfunctionMay 12, 2026Detachment of Device or Device Component

  THE END USER REPORTED THE HARDWARE FROM THE SEAT FRAME ASSEMBLY HAD LOOSENED AND CAME OUT. THERE WAS NO REPORT OF PATIENT INVOLVEMENT OR ASSOCIATED INCIDENT. THEY REQUESTED REPLACEMENT HARDWARE FOR THE OUT OF WARRANTY CHAIR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25149593 ↗
• MalfunctionJan 23, 2026Detachment of Device or Device Component

  THE END USER REPORTED WHEN THEY WERE REMOVING THE STAIR CHAIR FROM THE STORAGE LOCATION, THEY OBSERVED ONE OF THE TRANSPORT WHEELS HAD DETACHED. THERE WAS NO INJURY OR ADVERSE EVENT ASSOCIATED WITH THE REPORTED ISSUE. REPLACEMENT PARTS WERE PROVIDED. THE END USER CONFIRMED THE CHAIR HAS BEEN REPAIRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24161126 ↗
• MalfunctionJan 23, 2026Detachment of Device or Device Component

  THE END USER REPORTED ONE OF THE TRANSPORT WHEELS HAD DETACHED FROM THE STAIR CHAIR. NO ADDITIONAL DETAILS WERE PROVIDED AS TO HOW THE WHEEL BECAME DETACHED AND IF IT OCCURRED DURING A PATIENT TRANSPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24159341 ↗
• MalfunctionJan 8, 2026Detachment of Device or Device Component

  THE END USER REPORTED A TRANSPORT WHEEL ALLEGEDLY DETACHED FROM THE STAIR CHAIR. THE END USER STATED IT WAS NOTICED IN BETWEEN TRANSPORTS. THERE WAS NO ALLEGATION OF PATIENT INVOLVEMENT OR INJURY ASSOCIATED WITH THE REPORTED ISSUE. THE STAIR CHAIR WAS RETURNED TO MANUFACTURER FOR A VISUAL AND FUNCTIONAL EVALUATION. IT WAS CONFIRMED THE WHEEL OF THE CHAIR HAD NOT DETACHED BUT WAS LOOSE AND BEGINNING TO FALL OUT. REPLACEMENT WHEELS WERE INSTALLED ON THE CHAIR. THE CHAIR WAS CONFIRMED TO BE OPERATING ACCORDING TO SPECIFICATION AND WAS RETURNED TO THE END USER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24003588 ↗
• MalfunctionJan 8, 2026Detachment of Device or Device Component

  THE END USER REPORTED A TRANSPORT WHEEL ALLEGEDLY DETACHED FROM THE STAIR CHAIR. DETAILS OF WHEN THE ALLEGED PRODUCT ISSUE OCCURRED OR HOW THE CHAIR WAS BEING USED WAS NOT PROVIDED. THERE WAS NO ALLEGATION OF PATIENT INVOLVEMENT OR INJURY ASSOCIATED WITH THE REPORTED ISSUE. THE STAIR CHAIR WAS RETURNED TO MANUFACTURER FOR A VISUAL AND FUNCTIONAL EVALUATION AND THE ALLEGED ISSUE WAS CONFIRMED. A REPLACEMENT WHEEL WAS INSTALLED ON THE CHAIR. THE CHAIR WAS CONFIRMED TO BE OPERATING ACCORDING TO SPECIFICATION AND WAS RETURNED TO THE END USER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24003587 ↗
• MalfunctionJul 18, 2025Mechanical Problem; Mechanical Problem

  IT WAS REPORTED THE HARDWARE ON THE SEAT FRAME CAME LOOSE. THERE WAS NO PATIENT INCIDENT OR INJURY ASSOCIATED WITH THE ISSUE. REPLACEMENT HARDWARE WAS PROVIDED AND THE CHAIR WAS REPAIRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22546070 ↗
• MalfunctionJun 13, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THE FRONT WHEEL DETACHED FROM THE CHAIR. THERE WAS NO INCIDENT OR PATIENT INVOLVEMENT ASSOCIATED WITH THE REPORTED ISSUE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22205157 ↗
• MalfunctionJun 6, 2025Mechanical Problem; Mechanical Problem

  IT WAS FOUND DURING AN INSPECTION OF THE CHAIR THAT ONE OF THE TRANSPORT WHEELS HAD DETACHED FROM THE CHAIR. THERE WAS NO REPORT OF PATIENT INVOLVEMENT OR ADVERSE EVENT ASSOCIATED WITH THE REPORTED ISSUE. THE ISSUE WAS CONFIRMED VIA CONVERSATION WITH TECHNICAL SUPPORT AND REPLACEMENT PARTS WERE PROVIDED FOR THE REPAIR. THE CUSTOMER CONFIRMED THE REPAIR WAS COMPLETED AND THE CHAIR WAS RETURNED TO SERVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22157795 ↗
• MalfunctionMay 8, 2025Mechanical Problem; Mechanical Problem

  IT WAS REPORTED THE SEAT PANEL ASSEMBLY OF THE STAIR CHAIR WAS MISSING HARDWARE. THERE WAS NO REPORT OF ASSOCIATED PATIENT INVOLVEMENT, INJURY OR ADVERSE EVENT AS A RESULT OF THE REPORTED ISSUE. THE REPORTED ISSUE WAS CONFIRMED BY TECHNICAL SUPPORT AND REPLACEMENT PARTS WERE PROVIDED. THE CUSTOMER CONFIRMED THAT THE CHAIR WAS REPAIRED AND HAS BEEN RETURNED TO SERVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21986056 ↗
• MalfunctionMar 21, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED ONE OF THE FRONT TRANSPORT WHEELS ON THE CHAIR BECAME LOOSE AND DETACHED FROM THE FRAME DURING A PATIENT TRANSPORT. NO INJURIES OR ADVERSE EFFECTS WERE REPORTED AS A RESULT. THE CHAIR WAS EVALUATED BY AN AUTHORIZED FIELD TECHNICIAN AND THE ISSUE WAS CONFIRMED. IT WAS NOTED THE SHANK PIN ON THE WHEEL WAS BENT. THE CASTER WAS REPLACED AND THE CHAIR WAS RETURNED TO SERVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21667701 ↗
• MalfunctionMar 21, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED WHILE PUSHING A PATIENT ON THE CHAIR, ONE OF THE FRONT TRANSPORT WHEELS BECAME LOOSE AND DETACHED FROM THE FRAME. NO INJURIES OR ADVERSE EFFECTS WERE REPORTED AS A RESULT. THE STRETCHER WAS EVALUATED BY AN AUTHORIZED FIELD TECHNICIAN AND THE ISSUE WAS CONFIRMED. IT WAS NOTED THE SHANK PIN ON THE WHEEL WAS BENT. THE CASTER WAS REPLACED AND THE CHAIR WAS RETURNED TO SERVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21667700 ↗
• InjuryFeb 13, 2025Unintended Movement; Unintended Movement

  IT WAS REPORTED WHILE TRANSPORTING A PATIENT DOWN A FLIGHT OF STAIRS A BOLT IN THE SEAT FRAME ALLEGEDLY CAME LOOSE FROM THE FRAME RESULTING IN UNINTENDED MOVEMENT OF THE CHAIR. THE PATIENT WAS NOT INJURED BUT A MEDIC DID SUSTAIN A MINOR INJURY. DETAILS OF THE ALLEGED INJURY WERE NOT DISCLOSED. THE CHAIR WAS RETURNED TO THE MANUFACTURER FOR A VISUAL AND FUNCTIONAL EVALUATION. THE REPORTED ISSUE WAS CONFIRMED. THE CHAIR WAS REPAIRED AND RETURNED TO THE CUSTOMER.

  Patient problems: Insufficient Information

  MAUDE report 21374392 ↗