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Terumo Cardiovascular Systems Corporation recalls Cardiovascular Procedure Kit (CLR MP4 COIL 2 SPIKE) Catalog Number: 140222
Recalled March 6, 2019 · FDA recall Z-0966-2019 · Terumo Cardiovascular Systems
Hazard
Presence of natural rubber latex is not declared in the label · FDA Class II
Units
12 packs
Sold at
TX
Description
Presence of natural rubber latex is not declared in the label
Product
Cardiovascular Procedure Kit (CLR MP4 COIL 2 SPIKE) Catalog Number: 140222
Manufacturer(s)
Terumo Cardiovascular Systems Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →