Search results
Results From The WOW.Com Content Network
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]
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.
Here’s who needs to check their medicine cabinets
Metoprolol, sold under the brand name Lopressor among others, is a medication used to treat angina and a number of conditions involving an abnormally fast heart rate. [4] It is also used to prevent further heart problems after myocardial infarction and to prevent headaches in those with migraines . [ 4 ]
Experts explain why recalls aren't all bad and how consumers can protect themselves. ... Detwiler said, you should speak up if you see a staff member handling food who isn't being hygenic, such as ...
If you’re a wholesaler with recalled Prograf or Astagraf XL and have questions about the recall, call 877-575-3437, Monday through Friday, 9 a.m. to 5 p.m., Eastern time.
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. ... What is being recalled ...
(WJW) — A popular anxiety drug is being recalled over a ‘life-threatening’ label mistake. In a recall alert for some lots of Clonazepam Orally Disintegrating Tablets the FDA states the ...