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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.
0–9. 2007 Chinese export recalls; ... 2010 DePuy Hip Recall; 2010 Johnson & Johnson children's product recall; C. Chicago Tylenol murders; D. Drug recall; E.
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." [3] A McNeil spokesperson stated that the recall was not made on "the basis of adverse medical events ...
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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 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
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This event was linked to the death sentence of a former pharmaceuticals control officer in China, as the Costa Rican newspaper La Nación reported on its issue of May 30. [9] On June 4, 2007, a press release by the Chinese Foreign Ministry [10] cited an earlier study in China [11] which concluded that up to 15.6% diethylene glycol in toothpaste ...