:max_bytes(150000):strip_icc()/Health-tylenol-recall-b4942ad44d544ba294a09bca73268bd6.png?ssl=1 "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.
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