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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.
Kobayashi Pharmaceutical this week urged 52 manufacturers to recall a wide range of products such as tofu and miso which use beni koji that it supplies. Kobayashi Pharma ordered to recall red ...
First Aid Beauty initiated the recall of 2,756 jars of its bestselling Ultra Repair Intense Hydration cream on December 23 2024– a product known for its remedying effect on “dry, distressed ...
The recall comes after FDA investigators found unsterile conditions and "positive bacterial test results" at the facility where they are manufactured. Latest eye drop recall includes 27 products ...
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 FDA has announced over 20 recalls across the U.S., including food items, cosmetics, drugs, dietary supplements, and medical devices.
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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 ...