Kenvue Brands LLC recalls TYLENOL, Acetaminophen, Extra Strength, 24 Caplets, 500mg each, distributed by: Johnson & Johnson Consumer Inc., McNeil…
- Recall date
- October 21, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0121-2026
- FDA classification
- Class II
- Brand / firm
- Kenvue Brands LLC
- Sold / distributed
- U.S. Nationwide - CO, IL, OH and IN.
Why it was recalled
Defective Container
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was 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.
Get recall alerts
Free email alert whenever Kenvue Brands LLC has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Kenvue Brands LLC