Tylenol/Rolaids recall

[Dr Mordrid]

Link....

Tylenol Recall Broadens; Now Includes Tylenol Extra Strength, Rolaids

More Tylenol Products Recalled Due to Noxious Chemical

A recall of Tylenol products that began last month with the popular Tylenol arthritis caplet expanded this morning to include more than two dozen other over-the-counter products manufactured by McNeil Healthcare LLC, the arm of Johnson & Johnson that manufactures Tylenol products.

The broadened directive adds 54 million bottles of product to the recall, boosting the total number of bottles recalled by McNeil to 60 million, according to the company.

McNeill initiated a voluntary recall of Tylenol Arthritis Relief Caplets at the end of December after consumer complaints of stomach problems. The problems were linked to the presence of a chemical called 2,4,6-tribromoanisole (TBA), which results from the breakdown of a chemical in wood pallets used to transport and store packaging materials for the drugs.

Now it appears that the problem extended into other Tylenol products as well, according to the U.S. Food and Drug Administration.

Tylenol Extra Strength, Rolaids and a number of children's medicines are now included in the recall, which affects 27 products in various packaging quantities.

McNeil released a statement today in which it said the voluntary recall is being conducted in consultation with the FDA and affects a number of products for which there have been no complaints.

The company added that the musty-smelling chemical thought to be the cause of the sickness posed no fatal risk to those who ingest it.

"The health effects of this chemical have not been well studied, but no serious events have been documented in the medical literature," the statement read.

"In addition to the product recall, McNeil Consumer Healthcare is continuing its investigation into the issue and is taking further actions that include ceasing shipment of products produced using materials shipped on these wood pallets and requiring suppliers who ship materials to our plants to discontinue the use of these pallets."
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[Dr Mordrid]

Expanded.....

Tylenol recall expanded to Motrin, Benadryl, more

NEW YORK (AP) — Johnson & Johnson expanded a recall of over-the-counter medications Friday, the second time it has done so in less than a month because of a moldy smell that has made users sick.

The broadening recall now includes some batches of regular and extra-strength Tylenol, children's Tylenol, eight-hour Tylenol, Tylenol arthritis, Tylenol PM, children's Motrin, Motrin IB, Benadryl Rolaids, Simply Sleep and St. Joseph's aspirin. Caplet and geltab products sold in the Americas, the United Arab Emirates, and Fiji were recalled.

Johnson & Johnson's (JNJ) McNeil Consumer Healthcare Products recalled some Tylenol Arthritis Caplets in November due to the smell, which caused nausea, stomach pain, vomiting and diarrhea. Almost three weeks ago, the company expanded its recall to include Tylenol Arthritis Caplets.

The way the company handled the recall has irked federal regulators, who say McNeil did not act fast enough.

The Food and Drug Administration said McNeil knew of the problem in early 2008 but made only a limited investigation.

The agency said about 70 people were either sickened by the odor, or noticed it.

"McNeil should have acted faster," said Deborah Autor, the director of the FDA's Office of Compliance of the Center for Drug Evaluation and Research. "When something smells bad, literally or figuratively, companies must aggressively investigate and take all necessary action to solve the problem."
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