Almark Foods expands recall & suspends production over listeria concerns
What began as a ‘nationwide alert’ for hard boiled eggs by the U.S. Food and Drug Administration and Almark Foods, has now turned into a recall of not just hard boiled eggs but a large number of products produced at their Gainesville, Georgia facility. The expanded recall comes on the…
Possible E. coli contamination leads to Fresh Express Salad recall
Bags of Fresh Express Sunflower Crisp Chopped Salad Kits have been recalled by the U.S. Food and Drug Administration due to E. coli concerns. The recall comes after almost a dozen individuals in three states contracted E. coli shortly following consumption of the aforementioned Fresh Express salad kits.
FDA investigating diabetes drug ‘Metaformin’ over NDMA concerns
Stop us if you’ve heard this one before, there’s a concern over a carcinogen’s possible presence in a widely used medication. The only difference, this one has yet to be recalled, as the U.S. Food and Drug Administration is still investigating.
Listeria contamination concerns leads to White Castle frozen burger recall
If frozen White Castle burgers don’t sound like the most appetizing treat, today’s news will ensure you want avoid them altogether for some time. Five varieties of frozen burgers have been recalled due to a possible listeria contamination by White Castle and the U.S. Food and Drug Administration.
Breakstone Cottage Cheese recall issued due to “foreign material”
The U.S. Food and Drug Administration has issued a voluntary recall of select varieties of Breakstone Cottage Cheese due to the potential presence of foreign material. Pieces of red plastic and metal “may have been introduced during production” of 3 varieties of Breakstone’s cottage cheese.
FDA issues yellowfin tuna recall, company refuses to recall said tuna
A U.S. Food and Drug Administration recall is concerning enough. When is it an even bigger deal than normal? When the company that’s at the very heart of the recall refuses to recall the product. That’s the case right now with yellowfin tuna from a Vietnamese company called Truong Phu…
Despite the recall, the FDA wants consumers to know Zantac is relatively safe
Over the last few months, there have been numerous U.S. Food and Drug Administration recalls due to carcinogen concerns in heartburn medications. We’ve written about each of them here at TFF, and even posted an article just a couple weeks ago providing consumers with what the FDA considers “safe alternatives”…
Amid Zantac drug recall, FDA identifies “safe” heartburn drug alternatives
The popular heartburn medication Zantac has been recalled by the company and the U.S. Food and Drug Administration over N-Nitrosodimethylamine (NDMA) concerns. The recall began in the United States, and has reached Canada, Asia, and Europe. Initially, even the generic alternatives to Zantac were thought to be tainted, but it…
Dr. Reddy’s heartburn drug recalled over NDMA concerns
Dr. Reddy’s has joined the growing list of companies issuing a recall of heartburn medications. This week, Dr. Reddy’s Laboratories Ltd. and the U.S. Food and Drug Administration announced a recall of their “ranitidine medicines used to treat heartburn” after they were found to contain the carcinogen N-Nitrosodimethylamine aka NDMA.
Potential asbestos contamination leads to baby powder recall
Sample testing by the U.S. Food and Drug Administration of Johnson & Johnson talc-based baby powder uncovered an asbestos contamination. The presence of the cancer-causing chemical lead to a recall of more than 30,000 bottles of baby powder. So far, only baby powder has been recalled.