Reported Oct 12, 2016 · Terminated

Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is intended for use in removing arterial emboli.

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?

  • Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is intended for use in removing arterial emboli.
Lot codes and dates
    • Lot/Batch 14F15H0292
    • 14F15J0139
    • 14F15A0174
    • CF3016366
    • 14F14E0300
    • 14F15G0349
    • 14F15H0261
    • CF2079921
    • 14F15J0363
    • 14F14J0155
    • 14F15F0406
    • 14F15E0263
    • 14F15H0258
    • 14F15H0251
    • 14F15G0347. CF2125865
    • 14F15D0197
    • 14F15H0025
    • 14F15H0332
    • 14F15B0244
    • 14F15G0348
Amount recalled
2,425 catheters

Where it was sold

  • Nationwide

Why it was recalled

Arrow is recalling due to incorrect labeling of products.

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 Oct 25, 2017 · Data as of Sep 19, 4:44 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.