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May 26—A voluntary recall of Jif peanut butter that was announced Friday by the J.M. Smucker Co. because of potential Salmonella contamination was expanded Wednesday to include a list of candies ...
The full list is so extensive that the FDA created a separate page to track all the Jif-tainted products. However, even more recalls, including a ready-to-eat salad brand sold in Washington state ...
The recall now includes products sold under store brand names from retailers like Walmart, Safeway, and Albertson's. Jif's peanut butter recall has expanded to more than 100 products, including ...
This contamination triggered the most extensive food recall in U.S. history up to that time, involving 46 states, more than 360 companies, and more than 3,900 different products manufactured using PCA ingredients. The contamination and recall had immediate major ramifications for the market of this set of farm products.
Jif production plant in Lexington, Kentucky. The original Creamy and Crunchy style Jif peanut butters both made their nationwide debut in 1958. In 1974, Extra Crunchy Jif was introduced, followed in 1991 by Simply Jif, a peanut butter variant with low sodium and less sugar than regular Jif. Reduced Fat Jif was introduced three years later in ...
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
Information regarding product labels and the list of products will be provided when available. "The products subject to recall bear establishment numbers '51205 or P-51205' inside or under the ...
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.
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