(FORT WASHINGTON, PA) -- Tylenol has announced a recall of several types of its cold medicines in order to update labeling issues.
McNeil Consumer Healthcare, in consultation with the FDA, has announced the recall of several types of Tylenol Cold Multi-Symptom liquid products after a minor mislabeling of alcohol content was discovered.
The company said there is no need for consumers to stop using the product and no adverse events have been reported.
The following products are included in the recall:
Tylenol Cold Multi-Symptom Daytime 8oz Citrus Burst
Tylenol Cold Multi-Symptom Severe 8oz Cool Burst
Tylenol Cold Multi-Symptom Nighttime 8oz Cool Burst
All products were sold in the United States.
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