Curaplex 1613-862202Recalls & reported problems
Bound Tree Medical, LLC · Curaplex CuraSlide BC Safety IV Catheter w/ Blood Control, 20ga x 1in L, Pink · Class 2
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 00810094574178), received between Dec 27, 2024 and Dec 27, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Fragmentation” (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.
Reports received per month
Most reported problems
Device problems
- Material Fragmentation1
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.
MalfunctionDec 27, 2024Material Fragmentation; Material Fragmentation
MEDSOURCE RECEIVED FEEDBACK FROM OUR CUSTOMER STATING THAT: PROVIDER HAD INSERTED THE NEEDLE/CATHLON IN VEIN, FLASH DETECTED, STARTED ADVANCING CATHETER AND REMOVING NEEDLE. AFTER NEEDLE WAS REMOVED, CATHETER COULD NOT BE ADVANCED FURTHER TO PROPERLY PLACE CATHLON. WHEN PROVIDER WENT TO REMOVE CATHLON, IT TUGGED AT THE SKIN AND FINALLY CAME OUT WITH THE END LOOKING BUSTED OPEN. ADDITIONALLY, THEY STATED THAT THEY WERE NOT ABLE TO GET FLUIDS TO FLOW THROUGH THE PRODUCT. DUE TO THE POSSIBILITY OF CATHETER FRAGMENTS REMAINING IN THE VEIN FROM THE APPEARANCE THEY DESCRIBED IN THE COMPLAINT, IT WAS DETERMINED THAT THIS WAS A REPORTABLE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21026499 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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