Reported Apr 29, 2026 · Ongoing

ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J035…

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?

4 of 4 products

Products covered by this recall
Model / numberBarcodesProduct as published
ASK-04220-UCL110801902159127UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352
ASK-04020-EUH210801902213379UDI code: (01)10801902213379(17)270731(11)251218(10)33F25J0869
ASK-04020-FMC10801902212099UDI code: (01)10801902212099(17)270731(11)251218(10)33F25J0870
ASK-04020-MMC10801902117769UDI code: (01)10801902117769(17)271130(11)251211(10)33F25J0880 The Arrow Arterial Catheterization Device permits access to the peripheral arterial circulation or to other small vessels.
Lot codes and dates
  • Product codeASK-04220-UCL1
  • UDI code(01)10801902159127(17)270331(11)251203(10)33F25J0352
  • Batch Number33F25J0352
  • Product codeASK-04020-EUH2
  • UDI code(01)10801902213379(17)270731(11)251218(10)33F25J0869
  • Batch Number33F25J0869
  • Product codeASK-04020-FMC
  • UDI code(01)10801902212099(17)270731(11)251218(10)33F25J0870
  • Batch Number33F25J0870
  • Product codeASK-04020-MMC
  • UDI code(01)10801902117769(17)271130(11)251211(10)33F25J0880
  • Batch Number33F25J0880
Amount recalled
675

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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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 6:21 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.