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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 ...
2009, 84 Nigerian children were reported to have died after being given "My Pikin", a teething syrup contaminated with diethylene glycol. [ 18 ] 2012: As of 2 November 2012 [update] in the New England Compounding Center meningitis outbreak , 753 cases of fungal infection occurred with 64 deaths due to contaminated injectable medication.
On April 30, 2010, another recall was issued for 40 products including liquid infant and children's pain relievers Tylenol and Motrin, and allergy medications Zyrtec and Benadryl. [19] An FDA report said its inspectors found thick dust and grime covering certain equipment, a hole in the ceiling, and duct tape-covered pipes at the Fort ...
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Beyond its recall rate, CVS, which owns the health insurer Aetna, has struggled to bring in revenue due to high medical costs in the insurance industry as patients return to hospitals for more ...
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.
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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 ...