Tylenol and Motrin Recalled this 2010

The Food and Drug Administration says it is investigating after a health-care company recalled more than 40 over-the-counter infant’s and children’s liquid medications. The recall involves children’s versions of Tylenol, Tylenol Plus, Motrin, Zyrtec and Benadryl, because they don’t meet quality standards.

The FDA says the potential for serious medical problems is “remote,” but it is advising consumers to stop using the medicine.

Some of the products recalled may have a higher concentration of active ingredient than is specified on the bottle. Others may contain particles, while still others may contain inactive ingredients that do not meet internal testing requirements.

McNeil Consumer Healthcare is initiating this voluntary recall because 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.

Some of the products included in the recall may contain a higher concentration of active ingredient than is specified; others may contain inactive ingredients that may not meet internal testing requirements; and others may contain tiny particles. While the potential for serious medical events is remote, the company advises consumers who have purchased these recalled products to discontinue use.

McNeil offers a phone number for consumers to call: 1-888-222-6036 and on Monday through Friday 8 AM to 10 PM EST and Saturday and Sunday 9 AM to 5 PM EST. You can also visit the website www.mcneilproductrecall.com.

The medicines were made and distributed in the United States, and exported to Canada, the Dominican Republic, Dubai, Fiji, Guam, Guatemala, Jamaica, Puerto Rico, Panama, Trinidad and Tobago and Kuwait.

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