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Curaplex 3246-95206Recalls & reported problems

Bound Tree Medical, LLC · Curaplex Transport Chair · Class 1

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810071631450), received between Aug 25, 2023 and Aug 25, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (1 report).

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 16, 2026.

Most reported problems

Device problems

  • Material Split, Cut or Torn1

Patient problems

  • Unspecified Musculoskeletal problem1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 25, 2023Material Split, Cut or Torn; Material Split, Cut or Torn

    PARAMEDICS OPENED NEW TRANSPORT CHAIR AND ATTEMPTED TO LIFT PATIENT THAT IS DESCRIBED AS 230-240LBS WHEN PATIENT WAS PLACED IN THE CHAIR AND THEY ATTEMPTED TO LIFT AND MOVE THE TRANSPORTER CHAIR, THE TRANSPORT CHAIR RIPPED DOWN THE MIDDLE SEAM, CAUSING THE PATIENT TO DROP. THE MEDIC CAUGHT THE PATIENT TO EASE THE FALL. THE MEDIC'S ARM WAS INJURED, AND HE WAS PLACED OFF WORK.

    Patient problems: Unspecified Musculoskeletal problem

    MAUDE report 17628203 ↗

Other DEVICE, TRANSFER, PATIENT, MANUAL devices

All DEVICE, TRANSFER, PATIENT, MANUAL devices →

Sources and updates

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