FDADecember 20, 2018device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Presence of natural rubber latex is not declared in the label

What to do

FDA enforcement status: Terminated

Brands named

terumo cardiovascular systemsterumoterumo cardiovascular

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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