Acetaminophen Recall: Tylenol Extra Strength 24 Caplets 500 mg
Announced 2025-11-05 · FDA
Tylenol Extra Strength Acetaminophen 24 Caplets (500 mg) from Kenvue Brands LLC is recalled due to a defective container. About 3,816 bottles distributed nationwide in Colorado, Illinois, Ohio, and Indiana are affected. The affected lot is EJA022 with expiry date 04/30/2028.
| Brand | Kenvue Brands LLC |
|---|---|
| Product | 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. |
| Reason | Defective Container |
| Severity | moderate |
| Units affected | 3816 |
| Distribution | U.S. Nationwide - CO, IL, OH and IN. |
| Agency | FDA |
| Recall / campaign no. | Lot: EJA022, expiry: 04/30/2028 |
WHAT YOU SHOULD DO
- Stop using any Tylenol Extra Strength from lot EJA022.
- Check your bottle’s lot number and expiry date to see if it is EJA022 and expires 04/30/2028.
- Do not consume the product; contact Johnson & Johnson Consumer Inc. for return/replacement instructions or visit the recall page for guidance.
- If you have used the product and feel unwell, seek medical advice and report any adverse effects to a healthcare professional and the FDA.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.