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Found 7005 results for any of the keywords recalls market withdrawals. Time 0.011 seconds.

Recalls, Market Withdrawals, Safety Alerts | FDA

FDA and industry press releases regarding product recalls
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts - Details - Similar

U.S. Food and Drug Administration

The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of our nation s f
https://www.fda.gov/ - Details - Similar

Contact FDA | FDA

Contact information for the U.S. Food and Drug Administration.
https://www.fda.gov/about-fda/contact-fda - Details - Similar

Pennsylvania Personal Injury Lawyer - Lundy Law

Lundy Law is Pennsylvania Largest Personal Injury Law Firm. Jordan Lundy is a Pennsylvania Personal Injury Lawyer Winning over 1 billion.
https://www.lundylaw.com/ - Details - Similar

Food | FDA

Information from Humand Foods Program at FDA
https://www.fda.gov/food - Details - Similar

Animal Feed | Poisoned Pets | Pet Food Safety News

Cargill Inc. announced the recall of an astounding number of additional brands of animal feed this week, including horse feed, due to elevated aflatoxin levels. Aflatoxin is a toxin found ( ) Read more
https://www.poisonedpets.com/category/pet-product-recalls-alerts/animal-feed-recalls/ - Details - Similar

Pet Food | Poisoned Pets | Pet Food Safety News

A frantic pet parent contacted me recently, worried that the raw pet food they fed their cats made her cats violently ill. The pet food brand? Darwin s Natural Pet Products. ( ) Read more
https://www.poisonedpets.com/category/pet-product-recalls-alerts/cat-dog-food-recalls-alerts/ - Details - Similar

Generic Drug Facts | FDA

Information on how generic medicines have the same safety, effectiveness, and high quality as brand name medicines.
https://www.fda.gov/drugs/generic-drugs/generic-drug-facts - Details - Similar

MedWatch: The FDA Safety Information and Adverse Event Reporting Progr

MedWatch is made up of voluntary and mandatory reporting on prescription medicines, over-the-counter medicines, non-vaccine biologicals, medical devices, special nutritional products, cosmetics and non-prescription human
https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program - Details - Similar

Electronic Common Technical Document (eCTD) | FDA

Electronic Common Technical Document (eCTD) mandatory use for some submissions starts May 2017. eCTD is the standard format for electronic reg submissions.
https://www.fda.gov/drugs/electronic-regulatory-submission-and-review/electronic-common-technical-document-ectd - Details - Similar

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