ARROW CS-15192-VFIERecalls & reported problems
Teleflex Incorporated · Class 2 · Implant
Data updated Oct 13, 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 10801902154252), received between May 5, 2026 and May 5, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Difficult to Advance” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Difficult to Advance3
- Physical Resistance/Sticking3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 5, 2026Difficult to Advance; Physical Resistance/Sticking
IT WAS REPORTED THAT DURING INSERTION OF THE VECTORFLOW ANTEGRADE 19 CM CHDC, THE OPERATING PHYSICIAN ENCOUNTERED RESISTANCE WHILE ADVANCING THE CATHETER, WHICH WAS ATTRIBUTED TO THE CATHETER BEING PERCEIVED AS OVERLY STIFF AND RIGID. THERE WERE NO REPORTS OF PATIENT INJURY, HARM, OR ADVERSE HEALTH CONSEQUENCES ASSOCIATED WITH THIS EVENT. NO ADDITIONAL MEDICAL INTE RVENTION WAS REQUIRED, AND THE PROCEDURE WAS SUCCESSFULLY COMPLETED FOLLOWING REPLACEMENT OF THE DEVICE WITH AN ALTERNATIVE PRODUCT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25081141 ↗MalfunctionMay 5, 2026Difficult to Advance; Physical Resistance/Sticking
IT WAS REPORTED THAT DURING INSERTION OF THE VECTORFLOW ANTEGRADE 19 CM CHDC, THE OPERATING PHYSICIAN ENCOUNTERED RESISTANCE WHILE ADVANCING THE CATHETER, WHICH WAS ATTRIBUTED TO THE CATHETER BEING PERCEIVED AS OVERLY STIFF AND RIGID. THERE WERE NO REPORTS OF PATIENT INJURY, HARM, OR ADVERSE HEALTH CONSEQUENCES ASSOCIATED WITH THIS EVENT. NO ADDITIONAL MEDICAL INTERVENTION WAS REQUIRED, AND THE PROCEDURE WAS SUCCESSFULLY COMPLETED FOLLOWING REPLACEMENT OF THE DEVICE WITH AN ALTERNATIVE PRODUCT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25081080 ↗MalfunctionMay 5, 2026Difficult to Advance; Physical Resistance/Sticking
IT WAS REPORTED THAT DURING INSERTION OF THE VECTORFLOW ANTEGRADE 19 CM CHDC, THE OPERATING PHYSICIAN ENCOUNTERED RESISTANCE WHILE ADVANCING THE CATHETER, WHICH WAS ATTRIBUTED TO THE CATHETER BEING PERCEIVED AS OVERLY STIFF AND RIGID. THERE WERE NO REPORTS OF PATIENT INJURY, HARM, OR ADVERSE HEALTH CONSEQUENCES ASSOCIATED WITH THIS EVENT. NO ADDITIONAL MEDICAL INTERVENTION WAS REQUIRED, AND THE PROCEDURE WAS SUCCESSFULLY COMPLETED FOLLOWING REPLACEMENT OF THE DEVICE WITH AN ALTERNATIVE PRODUCT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25080982 ↗
Other Multi-lumen hemodialysis catheterization kit devices
- ARROW CS-15232-VFIETeleflex Incorporated · Multi-lumen hemodialysis catheterization kit2 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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