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Field Safety Notice Edwards Life sciences Intro-Flex Tuohy-Borst Valve Introducers Product Recall 2009-05-13 ATTENTION PLEASE DISTRIBUTE TO THE FOLLOWING DEPARTMENTS IN YOUR FACILITY: Surgery, Anesthesia,
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Urgent product recall refers to a swift and immediate action taken by a company to retrieve and remove a defective or unsafe product from the market.
The company responsible for manufacturing, distributing, or selling the product is usually required to initiate and file an urgent product recall.
The process of filling out an urgent product recall typically involves providing detailed information about the product, including its description, identification numbers, reason for recall, potential hazards, and corrective actions.
The purpose of urgent product recall is to protect consumers from potential harm or danger posed by a defective or hazardous product and to prevent any further distribution or sale of the product.
The information that must be reported on an urgent product recall includes product details, such as name, model, and serial numbers, identification codes, reason for recall, potential hazards, batch or lot numbers, distribution dates, and any corrective actions taken.
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