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FDA recalls more than 7,000 bottles of antidepressant

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,

USA TODAY on MSN · 1h

FDA recalls more than 7,000 bottles of antidepressant over a possible cancerous chemical

The FDA is recalling more than 7,000 bottles of the antidepressant duloxetine due to a possible cancer-causing chemical.

Health.com · 7m

FDA: Thousands of Bottles of Popular Antidepressant Recalled Over Potentially Cancer-Causing Chemical

Over 7,000 bottles of the antidepressant medication duloxetine, sold under the brand name Cymbalta, have been recalled, the FDA announced. The medication, produced by Towa Pharmaceutical Europe and distributed nationwide,

Frozen waffle recall expands

USA TODAY on MSN · 4h

Frozen waffle recall over listeria risk expanded to include pancakes: See affected products

TreeHouse Foods has expanded its voluntary recall of frozen waffle products to also include pancake products, the company announced Tuesday.

YAHOO!News · 6h

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 retailers across the United States and Canada. Walmart's Great Value, Target’s Good & Gather and Kodiak Power Waffles are among the frozen products recalled.

U.S. News & World Report · 1d

More Frozen Waffles and Pancakes Recalled Over Possible Listeria Contamination

This image provided by TreeHouse Foods, Inc., shows the packaging of two styles of waffles, among hundreds of brands of frozen waffles, that are part of a voluntary recall because the products could be contaminated with dangerous listeria bacteria,

8hon 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." ...

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 ...

Yahoo43m

The drug is manufactured by Towa Pharmaceutical Europe and was distributed nationally throughout the U.S., according to the FDA’s recall notice.

On today's episode of The College Football Enquirer, Dan Wetzel, Ross Dellenger and SI's Pat Forde unpack Texas' complicated ...

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 ...

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