Friday, January 14, 2011

Tylenol, Benadryl, Sudafed PE, Sinutab Recalls by Johnson & Johnson

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Johnson & Johnson Recalls Even More Medicines

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Just when it seemed pretty much impossible for Johnson & Johnson to recall even one more over-the-counter remedy, the company has shown it can.
The latest withdrawals, stemming from quality problems at a Pennsylvania factory, covers various batches of Tylenol 8 Hour, Tylenol Arthritis Pain, and Tylenol upper respiratory products made before last April. Also affected: some lots of Benadryl, Sudafed PE, and Sinutab.
  For more information and to see at a glance the remarkably broad array of medicines affected since trouble surfaced at the plant run by J&J's McNeil division last year, go to the company's dedicated recall website here.
The company has completed an investigation of quality problems at McNeil , maker of Tylenol and other over-the-counter medicines. The results showed, among other things, that the most recently recalled products may have been made on equipment that was dirty.In a statement, J&J said "an extensive review of past production records found instances where equipment cleaning procedures were insufficient or that cleaning was not adequately documented."
. Click Here to Read More.

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