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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.
Recalled Diet Coke has a best by date of 01/29/24, lot no. JAN2924MBD3, and UPC code 49000028911. Recalled Fanta Orange has the best by date of 07/29/24, lot no. JUL2924MBD3, and UPC code 49000030730.
Some bottles of the antidepressant duloxetine, sold under the brand name Cymbalta, were recalled due to the presence of a toxic chemical. Some bottles of the antidepressant duloxetine, sold under ...
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The Los Angeles Times headlined "Public Faces Overdose of Similar Drug Names." [14] The market for Zantac [15] and its competitors was described in 2005 as 13.5 billion US dollars. [16] The product's problem was described by The New York Times as being "that a potential cancer-causing contaminant can build up in the drug when stored for long ...
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.
Multiple vegetable medleys sold at retailers including Walmart and Sprouts Farmers Market are being recalled due to E. coli concerns. 4Earth Farms, a large California-based produce supplier ...
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]