Over 200,000 bottles of the antidepressant duloxetine have been recalled due to higher-than-acceptable levels of ...
FDA has announced a recall for Lay’s Classic Potato Chips on December 16, 2024, that may contain an undeclared milk allergen.
A New Jersey pharmaceutical company is recalling more than 230,000 bottles of duloxetine antidepressants after detecting a ...
It's the generic for one of the most-prescribed drugs treating the 21 million Americans who manage depression. Here's the ...
The FDA has recalled more than 233,000 bottles of antidepressant duloxetine, sold by Rising Pharmaceuticals, due to a potential cancer risk. The recall, issued Dec. 5, was prompted by the discovery of ...
More than 230,000 bottles of an antidepressant are being recalled. The medication contains levels of a chemical that pose a ...
An SNRI (serotonin and norepinephrine reuptake inhibitor) is one of two major classes of medications used to treat clinical ...
The FDA issued a second, expanded recall of duloxetine after higher than acceptable levels of a cancer-causing chemical were ...
In three separate reports, the FDA said that various doses of duloxetine delayed-release capsules were recalled due to the ...
The more than 233,000 bottles of duloxetine contain the "presence" of nitrosamine drug substance impurity, ...
The bottles were distributed nationwide, including in Wisconsin, and received the FDA's second-most severe risk ...
Cymbalta is used to treat mental health disorders. The bottles were distributed nationwide, according to the FDA.
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