FDA Drug · D-0121-2026

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.

Class II · Ongoing

Defective Container

Affected lots / codes — check yours against thisLot: EJA022, expiry: 04/30/2028

Recalling firm: Kenvue Brands LLC, Summitt, NJ
Classification: Class II (temporary or reversible harm possible)
Status: Ongoing
Quantity: 3,816 bottles
Distribution: U.S. Nationwide - CO, IL, OH and IN.
Recall initiated: October 21, 2025
Classified: October 28, 2025
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0121-2026%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

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