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Serious recall: Injury is possible or has been reported. Take action promptly.

Kenvue Brands LLC 2025-11-05 Health serious FDA
Health · FDA · Recall #FDA-D-0121-2026

TYLENOL, Acetaminophen, Extra Strength, 24 Caplets, 500mg each, distributed by: Johnson &… Recall

Issued November 5, 2025 · Kenvue Brands LLC

In November 2025, Kenvue Brands LLC recalled the TYLENOL, Acetaminophen, Extra Strength, 24 Caplets, 500mg each, distributed by: Johnson &…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Defective Container

What you should do

  1. 1 Stop using TYLENOL, Acetaminophen, Extra Strength, 24 Caplets, 500mg each, distributed by: Johnson &… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Kenvue Brands LLC to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Kenvue Brands LLC
Category
Health
Recall date
November 5, 2025
Units affected
Not reported
Sold at
U.S. Nationwide - CO, IL, OH and IN.
Recall number
FDA-D-0121-2026
Made in
United States
Issuing agency
FDA

In context

  • Kenvue Brands LLC has 1 recall in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 691st Health recall we've logged in 2025.
Read the official FDA notice

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