Curaplex 1613-86220Recalls & reported problems
Bound Tree Medical, LLC · Curaplex CuraSlide BC Safety IV Catheter w/ Blood Control, 20ga x 1-1/4in L, Pink · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00810094574185), received between Mar 27, 2025 and Jul 6, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Material Separation” (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. 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 Separation3
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Foreign Body In Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 6, 2026Material Separation
NO DAMAGE NOTED TO IV PACKAGING NOR IV ITSELF. NO DIFFICULTY IN ADVANCING NOR PLACEMENT; IT FLASHED, PATIENT GIVEN TWO ROUNDS OF MEDS WITH THREE TOTAL FLUSHES. UPON ADMINISTRATION OF THIRD NACL FLUSH, LEAKING WAS NOTED. WHEN THE HUB WAS CHECKED, IT WAS DETERMINED TO BE COMPLETELY DISCONNECTED FROM THE CANNULA. VCU REMOVED THE CANNULA AND NOTED A CLEAN DISCONNECTION AREA ON THE PROXIMAL END OF THE CANNULA WITH NO VISIBLE DAMAGE. PATIENT CARE WAS NOT DISRUPTED AND THEY WERE STILL IN THE CARE OF HOSPITAL STAFF ALIVE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25725974 ↗MalfunctionJul 30, 2025Material Separation; Material Separation
THE NEEDLE WAS STILL INSIDE THE CATHETER AFTER HITTING THE NEEDLE RETRACT BUTTON. THE CATHETER WAS INSIDE OF THE PATIENT'S ARM.
Patient problems: Foreign Body In Patient
MAUDE report 22669426 ↗MalfunctionMar 27, 2025Material Separation; Material Separation
THE CATHETER BODY WAS BROKEN INTO THE CATHETER HUB RESULTING IN NEEDLE EXPOSURE AFTER THE SAFETY MECHANISM WAS ACTIVATED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21713300 ↗
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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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