ARROW IPN920508Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10801902195460), received between Mar 18, 2026 and Mar 18, 2026 — classified as 1 malfunction.

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

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Apr 10, 2026Open, Classified

   16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.

   Z-2157-2026 · Root cause: Nonconforming Material/Component · FDA record ↗

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 18, 2026Fluid/Blood Leak

  IT WAS REPORTED THAT " THE BLUE VENOUS EXTENTION LINE ON THE HUB IS LEAKING AND PUSHES OUT AIR. THEY OPENED A NEW SET TO REMOVE AND USE HUB ASSEMBLY AND ALL WORKED WELL. "

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24626464 ↗