Reported Apr 29, 2026 · Ongoing

Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code:…

Arrow International, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: ARROW INTERNATIONAL, LLC · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437

Is this the product you have?

  • Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen
  • CVC Kit REF ASK-45854-PUPM1 UDI code(01)10801902159578(17)270531(11)251205(10)33F25M0011 The Arrowg+ard technology is intended to provide protection against catheter-related bloodstream infections (CRBSIs). It is not intended to be used as a treatment for existing infections nor is it indicated for long-term use (> 30 days). Clinical effectiveness of the Arrowg+ard Blue Plus catheter in preventing CRBSIs compared to the original Arrowg+ard Blue¿ catheter has not been studied
Lot codes and dates
  • Product CodeASK-45854-PUPM1
  • UDI code(01)10801902159578(17)270531(11)251205(10)33F25M0011
  • Batch Number33F25M0011
  • Product CodeASK-45703-MGH
  • UDI code(01)10801902223675(17)261231(11)251209(10)33F25L0143
  • Batch Number33F25L0143
  • Product CodeASK-42854-MGH
  • UDI code(01)10801902223668(17)261231(11)251210(10)33F25L0144
  • Batch Number33F25L0144
  • Product CodeASK-45854-MGH
  • UDI code(01)10801902223699(17)261231(11)251209(10)33F25L0145
  • Batch Number33F25L0145
Amount recalled
5

This recall covers 8 products

The agency filed one notice per product. You are reading one of them; the other 7 are below.

Where it was sold

Why it was recalled

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:41 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.