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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.
[3] [8] "A vast portion of the [American] children's medicine market" was affected by the recall. [3] In Canada, only Children's Motrin and Children's Tylenol Cough & Runny Nose were affected by the recall. [8] According to the FDA, consumers should stop using the recalled products even though the chance of related health problems was "remote."
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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 ...
The medicine was recalled in 2020 for the same reason.
The recalls come after news of at least seven reported illnesses in several states. 3 Applesauce Brands Recall Products After Kids Suffer 'Potential Acute Lead Toxicity' Skip to main content
2007 Toxic cough syrup in Panama: Pharmaceutical manufacturers used diethylene glycol, which they believed to be glycerine, to make cough syrup. [15] 2008 Chinese heparin adulteration [16] [17] 2009, 84 Nigerian children were reported to have died after being given "My Pikin", a teething syrup contaminated with diethylene glycol. [18]