FDA Pronounces Nationwide Tylenol Recall—Hundreds of Bottles Affected

A nationwide recall for about 3,000 bottles of Tylenol is underway, in accordance with the Meals and Drug Administration (FDA).

The ache reliever was initially recalled in mid-October as a result of a “faulty container,” and on Tuesday, the FDA gave the recall the second-highest threat degree, Class II.

This implies taking the recalled medicine could trigger “short-term or medically reversible antagonistic well being penalties,” or the opportunity of severe antagonistic well being results is “distant.”

The recalled Tylenol bottles may be recognized with the next:

Product description: TYLENOL, Acetaminophen, Additional Power, 24 caplets, 500 mg eachLot code: EJA022Expiry date: April 30, 2028

The three,186 recalled bottles have been distributed nationwide, however the FDA’s report particularly mentions Colorado, Illinois, Ohio, and Indiana within the product’s distribution sample.