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Get the free Class I Recall for Cordis' Super Torque Catheters ... - TCTMD

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Urgent FIELD AFTER NOTICE (CORRECTION) Cords SUPER TORQUE MB Angiographic Catheter×Catalog Numbers Modified Std Cat. Numbers 532598A 532598B 532598C SRD6875MB SRD7040MB NOTE: This is additional labeling.
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Class I recall is for products that have a high probability of causing serious adverse health consequences or death.
Manufacturers, distributors, or retailers of the recalled product are required to file a Class I recall.
Class I recall forms can be filled out online through the FDA's website or by submitting a written report.
The purpose of Class I recall is to quickly remove dangerous products from the market to protect public health.
Class I recall reports must include details about the product, the reason for the recall, the potential health risks, and the actions being taken.
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