Curaplex 3245-19123Recalls & reported problems
Bound Tree Medical, LLC · Curaplex Quick Connect Carrier · Class 1
Data updated Oct 18, 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 00817617029887), received between May 7, 2026 and May 7, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
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.
MalfunctionMay 7, 2026Break
THERE WERE TWO FEEDBACKS SUBMITTED FOR THE QUICK CONNECT CARRIER (3245-19123). BOTH FEEDBACKS INVOLVED THE CARRIER BREAKING AT A RIVET POINT. IN BOTH INSTANCES THERE WAS A PATIENT ON THE CARRIER, HOWEVER NEITHER INCIDENT INVOLVED AN INJURY DUE TO THE BREAKAGE OCCURING WHEN THE PATIENT WAS STILL VERY LOW TO THE GROUND. DUE TO THE POTENTIAL THAT AN INJURY COULD HAVE OCCURED A REPORT IS BEING FILED. BOTH INCIDENTS INVOLVED CARRIERS WITH VISIBLE WEAR/SCUFF MARKS. BOTH CARRIERS HAD 3-4 YEARS OF USE. THE LOT NUMBER COULD NOT BE IDENTIFIED FOR EITHER INCIDENT. FEEDBACKS WERE INITIALLY REPORTED TO THE DISTRIBUTOR AND THEN PASSED ALONG TO MEDSOURCE. THE INITIAL FEEDBACK REPORTERS TO THE DISTRIBUTOR ARE AS FOLLOWS: FB 1254 GONZALES CO EMERG 1703 N SAINT JOSEPH ST GONZALES, TX 78629-2331. FB 1269 AUDRIAN AMBULANCE DISTRICT 440 KELLEY PKWY MEXICO, MO 65265.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25117134 ↗
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 14781Bound Tree Medical, LLC · STRETCHER, HAND-CARRIED1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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