Curaplex 14781Recalls & reported problems
Bound Tree Medical, LLC · Curaplex Folding Scoop Stretcher, w/Straps (Load Limit 350lb) · Class 1
- 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 00812277037401), received between Jun 1, 2023 and Jun 1, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Premature Separation” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Premature Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 1, 2023Premature Separation; Premature Separation
FOLDING SCOOP STRETCHER LATCHES ARE OPENING WHEN WEIGHT IS APPLIED TO THE STRETCHER AND THE LATCH IS DEPRESSED. THIS WAS BROUGHT TO OUR ATTENTION BY A FEEDBACK RECEIVED STATING THAT THE PATIENT WAS BEING CARRIED DOWN THE STAIRS AND THEY SLID DOWN AND DEPRESSED THE LATCH WITH THEIR FEET CAUSING IT TO OPEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17043772 ↗
Other STRETCHER, HAND-CARRIED devices
- Transcend Chair Series 0731402Ferno-Washington, Inc. · Stretcher, Hand-Carried15 reports
- NA 6254Stryker Corporation · STRETCHER, HAND-CARRIED13 reports
- Transcend Chair Series 0731401Ferno-Washington, Inc. · Stretcher, Hand-Carried6 reports
- Curaplex 3245-19123Bound Tree Medical, LLC · STRETCHER, HAND-CARRIED1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.