Vicks Children's Botanicals Liquid Nighttime 4oz plastic bottle

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Batch Numbers: 0240C60404, 1166C60401, 1218C60401, 1237C60401, 1321C60401,1321C60402, 1321C604Q1, 2038C60401, 2152C60401 , 2153C60401 Lot Numbers: 0240C60404, 1166C60401, 1218C60401, 1237C60401, 1321C60401, 1321C60402, 1321C604Q1, 2038C60401, 2152C60401, 2153C60401 Product Number: 80338364 Item UPC: 323900041066 Case UPC: 10323900041063 Expiration Dates: 0240C60404 07/31/2022, 1166C60401 05/31/2023, 1218C60401 07/31/2023, 1237C60401 07/31/2023, 1321C60401 10/31/2023, 1321C60402 10/31/2023, 1321C604Q1 10/31/2023, 2038C60401 01/31/2024, 2152C60401 05/31/2024, 2153C60401 05/31/2024
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
The Procter & Gamble Company
Reason for Recall:
Acidified/Low Acid dietary supplement with no approved process.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Vicks Children's Botanicals Liquid Nighttime 4oz plastic bottle

Product Codes/Lot Numbers:

Batch Numbers: 0240C60404, 1166C60401, 1218C60401, 1237C60401, 1321C60401,1321C60402, 1321C604Q1, 2038C60401, 2152C60401 , 2153C60401 Lot Numbers: 0240C60404, 1166C60401, 1218C60401, 1237C60401, 1321C60401, 1321C60402, 1321C604Q1, 2038C60401, 2152C60401, 2153C60401 Product Number: 80338364 Item UPC: 323900041066 Case UPC: 10323900041063 Expiration Dates: 0240C60404 07/31/2022, 1166C60401 05/31/2023, 1218C60401 07/31/2023, 1237C60401 07/31/2023, 1321C60401 10/31/2023, 1321C60402 10/31/2023, 1321C604Q1 10/31/2023, 2038C60401 01/31/2024, 2152C60401 05/31/2024, 2153C60401 05/31/2024

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1535-2022

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