Reported Feb 28, 2018 · Terminated

Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous Catheterization Kit; Product Codes: ASK-45703-PNHS;…

Arrow International Inc.

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 Inc · 2400 Bernville Rd · Reading, PA · 19605-9607

Is this the product you have?

  • Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous Catheterization Kit
  • Product Codes
    • ASK-45703-PNHS
    • ASK-45703-PGMCL
    • ASK-45703-PNW
    • Exp. Dates Feb 2018 - Nov 2018
Lot codes and dates
  • Lot numbersProduct
  • Code ASK-45703-PNHS23F16M0498
  • Product Code ASK-45703-PGMCL23F17A0505
  • Product Code ASK-45703-PNW23F17B0116
Amount recalled
5,926 total

This recall covers 13 products

The agency filed one notice per product. You are reading one of them; the other 12 are below.

Where it was sold

  • Nationwide

Why it was recalled

These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Notice updated Apr 14, 2020 · Data as of Sep 19, 5:26 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.