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UPDATE 1-J&J recalls Benadryl, Tylenol overlooked in January
June 15, 2010 / 10:44 PM / 7 years ago

UPDATE 1-J&J recalls Benadryl, Tylenol overlooked in January

* 5 additional lots of over-the-counter products recalled

* J&J says were inadvertently missed in Jan. 15 recall

* House panel chairman says recalled lots adds to concern (Adds comments from House committee chairman, background)

By Ransdell Pierson

NEW YORK, June 15 (Reuters) - In another burst of bad publicity for Johnson & Johnson (JNJ.N), the company on Tuesday said it has recalled four additional lots of Benadryl allergy tablets and one lot of Extra Strength Tylenol gels.

The diversified healthcare company, in a press release, said it was recalling the lots after inadvertently failing to include them in a wider recall of over the counter drugs on January 15.

The company’s McNeil Consumer Healthcare unit said the latest action is a “follow-up” to the recall in January. On that occasion, 53 million bottles of a range of products were recalled after consumers complained of musty or moldy odors. The brands included Tylenol and Motrin painkillers, Rolaids, Benadryl and St. Joseph’s Aspirin.

All told, the J&J unit has issued four product recalls in the past year due to quality control problems at its plants, sparking a Congressional investigation and ongoing scrutiny by the U.S. Food and Administration.

“This latest recall is further evidence that there are wide-ranging problems at Johnson & Johnson,” Edolphus Towns, chairman of the U.S. House of Representatives Oversight and Government Reform Committee Chairman, said in a statement.

“I am troubled by what we have learned so far in our investigation and this latest development adds to my concern.”

J&J declined to comment on Towns’ statement.

The drugmaker said the odor that prompted its Jan. 15 recall was linked to traces of a chemical called TBA, caused by the breakdown of a chemical applied to wood used to build pallets that transport and store product packaging materials.

“Further analysis confirms that the risk of serious adverse medical events is remote,” J&J said on Tuesday.

J&J said the newly recalled lots -- made at a plant in Las Piedras, Puerto Rico -- were sold in the United States, Trinidad and Tobago, Bermuda and Puerto Rico.

One of McNeil’s two other main factories, located in Ft. Washington, Pennsylvania, has been shut down while the company strives to fix multiple deficiencies cited by the U.S. Food and Drug Administration.

“From a financial standpoint this really won’t have much of an impact on earnings, but it’s more of a concern to the strength of the Johnson & Johnson brand name,” said Morningstar analyst Damien Conover.

“With it being relatively few lots, that makes me a little bit less concerned,” Conover said. “That being said, you keep getting these red flags and you start to wonder.” (Reporting by Ransdell Pierson, Bill Berkrot and Susan Heavey; Editing by Steve Orlofsky and Richard Chang)

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