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Once all of a violative product has been removed from the market and all corrective and preventive actions (CAPAs) have been completed, a company can expect a formal end to a recall. Termination of a recall occurs once the FDA determines that a manufacturer has made all reasonable efforts to remove or correct the faulty product in accordance with the recall strategy and that it is reasonable to assume that the product has been removed and proper disposition or correction has been made commensurate with the degree of hazard posed by the product.