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Learn about the FDA's regulations and procedures for recalling or correcting medical devices that are in violation of laws or pose a risk to health. Find definitions, guidance, and federal ...
Find information about certain recalls of FDA-regulated products, such as food, drugs, medical devices, and cosmetics. Search by product type, date, brand name, or company name, and sign up to ...
Sec. 7.53 Recall status reports. (a) The recalling firm is requested to submit periodic recall status reports to the appropriate Food and Drug Administration district office so that the agency may assess the progress of the recall.
Find weekly reports, search features, and API for recalls of food, drugs, devices, and other products regulated by FDA. Learn about pending recalls, recall classifications, history, and subscriptions.
This chapter explains the FDA's responsibilities and procedures for initiating, classifying, monitoring, and terminating recalls of regulated products. It also provides attachments, exhibits, and ...
Find information on how to report, access, and monitor recalls of FDA-regulated products, such as drugs, devices, and food. Learn about industry and consumer resources, enforcement reports, and ...
Find medical device recalls classified by the FDA since November 2002, including corrections or removals initiated by firms. Search by product name, code, PMA/510 number, recall date, reason, firm, root cause and more.
The FDA Enforcement Report provides weekly and tailored reports of product recalls initiated by firms or requested by FDA. Learn how to access, search, view, and interpret the recall information ...
Learn how to report adverse reactions or other problems with FDA-regulated products, such as drugs, medical devices, and vaccines. Find online forms, instructions, and links for consumers, health ...
You should submit periodic recall status reports to the appropriate FDA district office so that we may assess the progress of the recall [21 CFR 7.53]