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FDA, recall
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.
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.
Juice Drinks Recall Update as FDA Sets Risk Level
In an update issued on Tuesday, the FDA classed the recalls as Class II, which is when the "use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote."
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
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.
Thousands of bottles of common antidepressant Cymbalta recalled by FDA over cancer-causing chemical
Thousands of bottles of a commonly prescribed antidepressant drug have been recalled by the FDA because they were found to contain a suspected cancer-causing chemical. Over 7,100 bottles of Duloxetine,
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.
2h
on MSN
Dog Medicine Recall Update As FDA Sets Risk Class
A class II risk level is given to products that "may cause temporary or medically reversible adverse health consequences." ...
38m
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 ...
2d
on MSN
Listeria contamination prompts recall of generic waffle brands at retailers across U.S., FDA says
Generic waffle brands at retailers across the U.S. are being recalled after listeria, a potentially fatal bacterial disease, ...
Newsweek
1d
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 ...
12d
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 ...
KOLR Springfield on MSN
17h
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 ...
al.com
13d
Check your fridge for these brands: FDA has upgraded its recall on eggs
The Food and Drug Administration has escalated an ongoing egg
recall
to its most serious class. On Sept. 6, the Centers for ...
1d
on MSN
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 ...
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Duloxetine
listeria
antidepressant
United States
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