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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 company's share price has fallen nearly 20% since Friday when it first issued a voluntary recall of its own supplements. On Wednesday, they closed down 3.8% at 4,875 yen.
The FDA has announced over 20 recalls across the U.S., including food items, cosmetics, drugs, dietary supplements, and medical devices.
U.S. health officials recalled three more brands of whole and pre-cut cantaloupes Friday as the number of people sickened by salmonella more than doubled this week.. Nearly 100 people in 32 states ...
This contamination was not detected until 2018. The incident, according to medicinal chemist and pharmaceutical industry blogger Dr. Derek Lowe, points to a greater problem. Generic drug manufacturers often change the way in which prescription drug ingredients are made in order to lower costs of making them, so this kind of contamination may be ...
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.
A RaceTrac fruit-in-plastic item is also included among the three new recalls in a 15-state outbreak. Latest salmonella outbreak recalls include whole cantaloupes and Walmart fruit dishes Skip to ...
The recall stems from potential salmonella contamination. Affected bags have an expiration date of Oct. 30, 2026, and the lot number 24095 C018 printed on the bottom of the back panel . No ...