The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. See FDA’s role in drug recalls for more information. The U.S. Food and Drug Administration has issued a recall of Sportmix pet food products that have been linked to multiple dog deaths, the organization announced Wednesday. Drug recalls are actions taken by a firm to remove a product from the market and may be conducted on a firm's own initiative, by FDA request, or by FDA order under statutory authority. The FDA is not required to publicly recall … The recalled products have U.S. Food and Drug Administration (FDA) approval and in many cases, are widely ingested, injected or implanted before being recalled. (g) Recall means a firm's removal or correction of a marketed product that the Food and Drug Administration considers to be in violation of the laws it administers and against which the agency would initiate legal action, e.g., seizure. September 21, 2020 -- The U.S. Food and Drug Administration is alerting health care professionals and patients of a voluntary recall of all unexpired albuterol... September 21, 2020 Acella Pharmaceuticals, LLC Issues Voluntary Nationwide Recall of Two Lots of … Medication Guides, Drug Safety Communications, Shortages, Recalls. For recall notices older than 60 days, see recall and safety alerts archive. Recalls may stem from things such as incorrect ingredient levels, the use of undeclared or unapproved drugs, or contamination. Source: FDA Legacy Pharmaceutical Packaging, LLC Issues Voluntary Nationwide Recall of Losartan Potassium Tablets, USP, 25mg, 50mg, And 100mg Due to The Detection of Trace Amounts Of N-Nitroso N-Methyl 4-Amino Butyric Acid (NMBA) Impurity Found in The Active Pharmaceutical Ingredient (API) Enroll in this free service by signing up for direct notification of recalls from the U.S. Consumer Product Safety Commission, the Food & Drug Administration and the U.S. Department of Agriculture. Some FDA recalls may apply to products that result in lawsuits for injury or economic harm to a consumer or patient. We comply with the HONcode standard for trustworthy health information -, Sunstar Americas Inc. The following FDA safety notices may be specifically about metformin or relate to a group or class of drugs which include metformin. The FDA may also request that a manufacturer recall a drug on a voluntary basis if it receives enough evidence to warrant a recall. Besides drugs, foods, and cosmetics, an FDA Recall can also apply to: vaccines; human tissue used for transplantation; human blood and blood products, and; medical devices. The .gov means it’s official.Federal government websites often end in .gov or .mil. The Food and Drug Administration's (FDA) rolling list of potentially dangerous hand sanitizers has just expanded -- again. § 7.46 - Firm-initiated recall. FDA tested product; contains methanol; FDA recommended the company recall on … * Drugs@FDA includes information about drugs, including biological products, approved for human use in the United States (see FAQ), but does not include information about FDA-approved products regulated by the Center for Biologics Evaluation and Research (for example, vaccines, allergenic products, blood and blood products, plasma derivatives, cellular and gene therapy products). provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. Sildenafil is the active ingredient in popular erectile dysfunction treatments, while trazodone hydrochloride is indicated for the treatment of major depressive disorders.