TRANSCEND 0731405Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00190790006334), received between Jul 23, 2025 and Feb 25, 2026 — classified as 1 injury, 3 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (3 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.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 25, 2026Mechanical Problem; Detachment of Device or Device Component

  THE END USER REPORTED WHILE MOVING A PATIENT ON THE STAIR CHAIR, A BOLT DETACHED FROM THE SEAT FRAME ASSEMBLY. THERE WERE NO INJURIES REPORTED AS A RESULT OF THE REPORTED ISSUE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24446540 ↗
• InjuryFeb 3, 2026Unintended Movement

  IT WAS REPORTED WHILE TRANSPORTING A PATIENT DOWN STAIRS, THE PISTON ON THE TRACK ASSEMBLY BROKE AWAY FROM THE CHAIR RESULTING IN UNINTENDED MOVEMENT OF THE TRACK ASSEMBLY AND THE ATTENDING MEDICS HAD TO SUDDENLY CATCH THE CHAIR TO CONTROL ITS MOVEMENT. THERE WERE NO INJURIES TO THE PATIENT; HOWEVER, BOTH MEDICS ALLEGED MUSCLE STRAIN TO THEIR BACK AND ONE MEDIC ALSO ALLEGED SHOULDER STRAIN. NEITHER MEDIC SOUGHT MEDICAL INTERVENTION BUT RATHER REQUIRED REST FOLOWING THE INCIDENT. THE END USER ADVISED THEY HAVE REPORTED THIS INCIDENT ON A MEDSUN REPORT. THE CUSTOMER PROVIDED IMAGES OF THE CHAIR AND THE ALLEGED ISSUE WAS ABLE TO BE CONFIRMED. REPLACEMENT PARTS WERE PROVIDED TO THE END USER AS THEY ARE AN AUTHORIZED FIELD TECHNICIAN. THE END USER CONFIRMED THE CHAIR HAS BEEN REPAIRED AND RETURNED TO SERVICE. THE REPLACED GAS SPRING HAS BEEN RETURNED TO THE MANUFACTURER FOR FURTHER ANALYSIS.

  Patient problems: Muscle/Tendon Damage

  MAUDE report 24247184 ↗
• MalfunctionDec 24, 2025Mechanical Problem; Mechanical Problem

  THE END USER REPORTED MISSING HARDWARE FROM THE ASSEMBLY CONNECTING THE SEAT FRAME TO THE MAINFRAME OF THE CHAIR. THIS OBERSVATION WAS MADE DURING INSPECTION AND THERE WAS NO ADVERSE EVENT OR INJURY ASSOCIATED WITH THE PRODUCT ISSUE. REPLACEMENT HARDWARE WAS SENT TO THE CUSTOMER FOR INSTALLATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23888584 ↗
• MalfunctionJul 23, 2025Mechanical Problem; Mechanical Problem

  IT WAS REPORTED THE HARDWARE ATTACHING THE SEAT FRAME TO THE MAINFRAME OF THE CHAIR HAD BACKED OUT OF POSITION. THERE WAS NO PATIENT INVOLVEMENT OR INJURY ASSOCIATED WITH THE REPORTED ISSUE. THE ISSUE WAS CONFIRMED VIA COMMUNICATIONS WITH THE END USER AND REPLACEMENT PARTS WERE PROVIDED FOR REPAIR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22579130 ↗