Reported Jun 6, 2018 · Terminated

ARROWg+ard Blue PLUS¿ Pressure Injectable Quad-Lumen CVC Kit; Product Codes: CDC-42854-P1A and CDC-45854-P1A

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?

  • ARROWg+ard Blue PLUS¿ Pressure Injectable Quad-Lumen CVC Kit
  • Product CodesCDC-42854-P1A and CDC-45854-P1A
Lot codes and dates
  • Lot numbersProduct
  • code CDC-42854-P1A
    • 13F17C0137
    • 13F17E0177
    • 13F17E0598
    • 13F17F0644
    • 13F17G0287
    • 13F17H0118
    • 13F17K0156
    • 13F17L0017
    • 13F17M0158
  • Product code CDC-45854-P1A
    • 13F17C0396
    • 13F17C0439
    • 13F17D0062
    • 13F17D0284
    • 13F17E0618
    • 13F17F0126
    • 13F17G0293
    • 13F17H0263
    • 13F17J0055
    • 13F17K0168
    • 13F17L0021
    • 13F17L0353
    • 13F17L0590
Amount recalled
416,055 total products

This recall covers 76 products

The agency filed one notice per product. You are reading one of them; the other 75 are below.

63 more are in the archive.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Product sterility may be compromised due to unsealed packaging.

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

Notice updated May 15, 2020 · Data as of Sep 19, 5:30 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.