ARROW CS-15272-VFERecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10801902154207), received between Mar 9, 2026 and Mar 9, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fluid/Blood Leak” (1 report).

1 other recall cover devices cleared under the same FDA submission (K141051); they may or may not involve this specific model.

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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 9, 2026Fluid/Blood Leak; Incomplete or Inadequate Connection

  IT WAS REPORTED THAT: "BLOOD WAS FOUND LEAKING FROM THE HUB CONNECTION ASSEMBLY AFTER INSERTION OF THE CATHETER. THEREFORE, THE CATHETER WAS REMOVED AND REPLACED WITH A NEW ONE. NO INJURY TO THE PATIENT OCCURRED. ACCORDING TO THE USER, THE COMPRESSION SLEEVE COULD NOT BE PLACED ONTO THE CATHETER SHAFT FIRMLY SO HE/SHE SUSPECTED THE PRODUCT SHAPE MIGHT HAVE BEEN DEFECTIVE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24543122 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K141051. One submission often covers many models, so check the product and lot details in each record.

• Z-2157-2026 · Apr 10, 2026 · Open, Classified
  Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-VFI, ACS-15232-VFI, ACS-15272-VFI, CS-15192-VFI, CS-15192-VFIE, CS-15232-VFI, CS-15232-VFIE, CS-15272