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Baby Aspirin Recalled Over Acetaminophen Mix-Up

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Courtesy: FDA

LOS ANGELES (KTLA) — A major medication mix-up prompted the nationwide recall Friday of 16,440 bottles of baby aspirin.

Advance Pharmaceutical Inc. issued a recall of its Rugby label Enteric Coated Aspirin, 81-mg tablets, after a CVS pharmacist discovered a bottle filled with 500- milligram acetaminophen pills, according to a statement from the Food and Drug Administration.

Doctors often prescribe low-dose aspirin to patients at a high risk for heart attack or stroke.

Low-dose aspirin is also commonly given to patients following surgery to prevent clotting.

Taking acetaminophen, often sold under the brand name Tylenol, at a high dose “may cause severe liver damage to those who take other drugs containing acetaminophen, consumers who take three or more alcoholic drinks every day, or those who have liver disease,” according to the FDA.

Consumers who purchased bottles with a lot no. 13A026 and expiration date of January, 2015 were asked to immediately discontinue use and return the medicine to the pharmacy or store where it was bought.

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