FDA, recall

FDA Has Recalled Thousands of Bottles of Antidepressant Duloxetine, Sold Under Brand Name Cymbalta: Here’s Why
The U.S. Food and Drug Administration has recalled thousands of bottles of the antidepressant Duloxetine (sold under the brand name Cymbalta) for potentially cancer-causing chemicals in the medication.
FDA issues recall for antidepressant drug
The Federal Drug Administration issued a recall on Tuesday for a common medicine for depression. Over 7,000 bottles of Duloxetine were recalled due to the elevated presence of Nitrosamine, an ingredient believed to be cancerous,
7,100 bottles of antidepressant recalled by FDA now in 2nd highest risk class
Duloxetine Delayed-Release Capsules were recalled because the pills may contain high levels of a cancer-causing chemical.
Antidepressant recall: FDA upgrades medication risk class to 2nd highest level in recall update
The U.S. Food and Drug Administration is urging patients not to stop taking their prescribed medication if it falls under the recall but instead to address any concerns and other potential treatment o
Nationwide Antidepressant Recall Update As FDA Sets Risk Class
The recall of the Duloxetine Delayed-Release Capsules, produced by Towa Pharmaceutical Europe, was initiated on October 10 and has been given the second highest risk classification by the FDA. Duloxetine is a medication used to manage depression,
Duloxetine antidepressant recalled over presence of toxic chemical
Some bottles of the antidepressant duloxetine, sold under the brand name Cymbalta, were recalled due to the presence of a toxic chemical.
Antidepressant recalled: 2nd-highest FDA risk level; drug contains cancerous chemical
The U.S. Food and Drug Administration updated the risk level of a recalled antidepressant due to the product containing high levels of a cancer-causing chemical.
Vegetable Recall Update: Warning for State As FDA Sets Highest Risk Level
The vegetable products were recalled due to a possible contamination with the bacteria Listeria monocytogenes.
FDA Recalls Thousands Of Duloxetine Antidepressant Bottles | Here's Why
The US Food and Drug Administration has recalled thousands of bottles of Duloxetine antidepressant, saying it contained high levels of a cancer-causing chemical. The federal agency has reportedly upgraded the level of risk.
Antidepressant recall: FDA upgrades risk level due to cancer-causing chemical
After the U.S. Food and Drug Administration recalled thousands of bottles of antidepressants it said contained high levels of a cancer-causing chemical, the federal agency has now upgraded the level of risk.
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Milk Recall Update As FDA Sets Highest Risk Level
The U.S. Food and Drug Administration (FDA) has issued a Class I recall for a line of milk products as they may contain undeclared almonds from almond milk, a known allergen. The firm-initiated ...
Walmart and Target Recall Frozen Waffles Due to Listeria—Check Your Kitchen Now
Many frozen waffle brands distributed by TreeHouse Foods have been recalled due to listeria contamination at various major ...
Consumers asked to throw away millions of eggs as FDA upgrades recall status to most serious category
The FDA announced that the recall of "Milo’s Poultry Farms" and "Tony’s Fresh Market" has been upgraded to Class I, meaning ...
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LIST: Waffles, pancakes recall expanded over potential listeria contamination
Last week, the FDA announced a limited voluntary recall by TreeHouse Foods of more than 500 varieties of frozen waffles sold ...
FDA says egg recall over salmonella can have 'serious' health effects: Avoid these brands
Eggs sold in three states have been recalled due to possible salmonella contamination. Here's what consumers need to know ...
FDA upgrades ongoing egg recall to Class 1 following multi-state Salmonella outbreak
Nearly a month after the Food and Drug Administration (FDA) issued an initial recall of eggs produced by a Wisconsin-based ...
Wisconsin Trader Joe’s stores recall green onions over potential salmonella contamination
Produce distributor Church Brothers Farms voluntarily recalled its green onions with the U.S. Food and Drug Administration ...
Cheeseburger recall: FDA says three prepared burgers may contain listeria
Burger lovers, beware: An FDA recall is pulling these prepared cheeseburgers from shelves due to a potential listeria ...