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Moog's primary products are electronic ambulatory infusion pumps and ambulatory enteral feeding pumps along with the necessary administration sets as well as disposable infusion pumps. Applications of these products include controlled delivery of fluids to the body, nutrition, post-operative pain management, regional anesthesia, chemotherapy ...
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.
The recall by the U.S. Food and Drug Administration of one medical company's entire line of infusion pumps -- widely used to administer fluids to the human body -- has called attention to ...
The recalls came in response to reports of renal failure in pets consuming mostly wet pet foods made with wheat gluten from a single Chinese company, beginning in February 2007. The recall began voluntarily with the Canadian company Menu Foods on March 16, 2007, when a company test showed sickness and death in some of the test animals. Overall ...
Several recalls were issued in 2024 for Ford Motor Company vehicles. The recall report data is from Jan. 1, 2024, to Dec. 27, 2024. The U.S. Department of Transportation (DOT) compiles data from ...
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2007 pet food recalls; 2008 Irish pork crisis; 2008 Chinese milk scandal; 2009 Peanut Corporation of America recall; 2009 peanut recall; 2012 outbreak of Salmonella; 2013 Fonterra recall; 2013 horse meat scandal; 2022 United States infant formula shortage; 2024 McDonald's E. coli outbreak; 2024 United Kingdom Shigatoxigenic E. coli outbreak
Ford Motor is recalling 295,449 diesel-engine trucks because a defective fuel pump could cause a loss of ... or go to www.nhtsa.gov for further information. NHTSA's number for the recall is 24V-957.