BENADRYL, SINUTAB, SUDAFED PE, And Tylenol, Reacalled By McNeil Consumer Healthcare.

 McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc. has recalled, certain lots of TYLENOL® 8 Hour, TYLENOL® Arthritis Pain, and TYLENOL® upper respiratory products, and certain lots of BENADRYL®, SUDAFED PE®, and SINUTAB® products distributed in the United States.
Recallr: McNeil Consumer Healthcare Recalls TYLENOL® 8 Hour, TYLENOL® Arthritis Pain, and TYLENOL® upper respiratory products, And BENADRYL®, SUDAFED PE®, and SINUTAB® products.

McNeil Consumer Healthcare Recalls over-the-counter (OTC) Children’s and Infants’ liquid products including Tylenol, Motrin, Zyrtec, and Benadryl products

[Posted 04/30/2010] McNeil Consumer Healthcare and FDA notified healthcare professionals of a voluntary recall of certain over-the-counter (OTC) Children’s and Infants’ liquid products manufactured in the United States, including Tylenol, Motrin, Zyrtec, and Benadryl products. Some of these products may not meet required quality standards. This recall is not being undertaken on the basis of adverse medical events. However, as a precautionary measure, parents and caregivers should not administer these products to their children. These products were distributed in the United States, Canada, Dominican Republic, Dubai (UAE), Fiji, Guam, Guatemala, Jamaica, Puerto Rico, Panama, Trinidad & Tobago, and Kuwait. Consumers can contact the company at 1-888-222-6036 and also at www.mcneilproductrecall.com
[04/30/2010 - Questions and Answers¹ - FDA]