United StatesTYLENOL Extra Strength acetaminophen 500 mg, 24 caplets (NDC 50580-378-04), lot EJA022, expiry 04/30/2028, distributed by Johnson & Johnson Consumer Inc./McNeil and recalled by Kenvue Brands LLC. It was recalled due to a defective container; 3,816 bottles were distributed nationwide, including Colorado, Illinois, Ohio and Indiana.
What's being recalled
TYLENOL, Acetaminophen, Extra Strength, 24 Caplets, 500mg each, distributed by: Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division, Fort Washington, PA 19034, NDC: 50580-378-04.
Recalling firm: Kenvue Brands LLC, Summitt, NJ, United States.
How to identify it
Lot: EJA022, expiry: 04/30/2028
The hazard
Defective Container
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
U.S. Nationwide - CO, IL, OH and IN.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)