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The FDA has recalled thousands of bottles of the antidepressant duloxetine, sold under brand name Cymbalta, due to the presence of a possibly cancer-causing chemical.
The recall covers 7,107 bottles of duloxetine, the FDA said. The bottles include 500 delayed-release 20mg capsules. The lot number is 220128, with an expiration date of 12/2024.
The U.S. Food and Drug Administration has recalled thousands of bottles of the antidepressant Duloxetine for potentially cancer-causing chemicals above the acceptable limit set by the FDA, per the ...
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.
The Food and Drug Administration announced a Class II recall for more than 7,000 bottles of an antidepressant due to a chemical.. The recall was initiated earlier this month on Oct. 10. Duloxetine ...
Bayer recalls one lot of cancer drug Vitrakvi due to contamination. November 17, 2023 at 8:19 PM ... The recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
For questions about this recall, contact 4Earth Farms at 855-918-1706, Monday through Friday from 8 a.m. to 4:30 p.m. PT. Related: Cucumbers Sold at Costco, Walmart and More Recalled Nationwide ...
IHA Beverage issued a voluntary recall for Super Cinnamon Powder due to elevated lead levels. The Food and Drug Administration (FDA) issued the recall alert on Monday, Nov. 18. The brand for the ...