Reported Mar 6, 2019 · Terminated

Cardiovascular Procedure Kit (CLR MP4 COIL 2 SPIKE) Catalog Number: 140222

Terumo Cardiovascular Systems Corporation

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: Terumo Cardiovascular Systems Corporation · 125 Blue Ball Rd · Elkton, MD · 21921-5315

Is this the product you have?

  • Cardiovascular Procedure Kit (CLR
  • MP4 COIL 2 SPIKE) Catalog Number140222
Lot codes and dates
  • Lot NumbersV A30
Amount recalled
12 packs

Where it was sold

Why it was recalled

Presence of natural rubber latex is not declared in the label

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 Aug 20, 2019 · Data as of Sep 19, 6:57 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.