Extra-strength acetaminophen recalled nationwide Courtesy of FDA Nearly 200,000 bottles of extra-strength acetaminophen, used to relieve pain and fevers and sold under multiple brand names, are being recalled nationwide due to a mislabeling issue. A-S Medication Solutions, LLM voluntarily recalled bottles of its Acetaminophen Extra Strength 500 mg tablets because they have "an incomplete prescription drug label rather than the required OTC Drug Facts label," the Food and Drug Administration (FDA) said in a notice. Representatives for A-S Medication Solutions did not return FOX Business' request for comment. Advertisement The proper label is supposed to include warnings about "liver damage if consumers exceed the recommended dose, combine use with excessive consumption of alcohol" or if consumers "are allergic to the active ingredient."