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: Illinois Injury Lawyer BlogTylenol plant conditions called ?shocking?
Recent findings are showing that the safety and quality violations that led to the Tylenol plant shutdown were extremely serious and can lead to extremely tough action by United States regulators on drugmaker Johnson & Johnson. Last week, the Food and Drug Administration (?FDA?) released an inspection report on the facility in Pennsylvania where the product recall stems from, which a professor of pharmaceutical manufacturer called ?absolutely shocking.? According to the professor at Temple University, the inspection report ?is pretty close to being the worst [he?s] seen. It suggests that basically the FDA found an issue with almost every system at the plant.?
Earlier this month, a division of Johnson & Johnson recalled nearly fifty children?s versions of non-prescription (over-the-counter) drugs, including Tylenol, Motrin, and Benadryl. Since then, Johnson & Johnson has suspended all production at the plant. The FDA report listed twenty violations, including dozens of consumer complaints on the products recalled. However, Johnson & Johnson has not revealed details of those complaints. Congress has opened a product liability investigation into the product recall and lawmakers gave Johnson & Johnson and the FDA a deadline of today (May 17) to hand over details about consumer complaints. The Illinois product liability attorneys will keep our readers posted as the details of this product recall involving millions of consumers unfolds.
Chicago injury attorneys at Levin & Perconti want to remind you that you can dispose of pharmaceuticals. The City of Chicago and the Chicago Police Department have partnered to provide a place for the safe and proper disposal of unused or expired prescription and over-the-counter medications.
Where to dispose of recalled and expired prescription and over-the-counter medications.
To read about the shocking conditions at the product facility.
Full post as published by Illinois Injury Lawyer Blog on May 17, 2010 (boomark / email).
Recall of TYLENOL 8 Hour Caplets 50 Count Sold in The United States and Puerto Rico
TYLENOL 8 Hour Caplets 50 Count One Lot Recalled in US and Puerto Rico
Nationwide Recall Of All Lots Of Tylenol Arthritis Pain 100 Count With Ez-Open Cap
Tylenol Arthritis Pain 100 Count With Ez-Open Cap All Lots Recalled Nationally
Brinker International
allegedly falsely advertising the nutritional information on their so-called low calorie menu selections.
Oil and Gas
industry workers allegedly subject to serious accident injury from hazardous conditions.
Tylenol
Linked to Risk of Asthma in Children
Pre-Existing Conditions
Insurance companies to pay over $2.1 million settlement in claims lawsuit.

No news in the Tylenol poisoning case
FDA: Tylenol Factory Conditions Unacceptable
Recall of Tylenol Arthritis Pain Caplets Expanded
Johnson & Johnson Recalls Children's Tylenol Products
Expanded Recall of Tylenol Arthritis Product
UK food plant shut down after filthy conditions discovered








