Vicks Children's Botanicals Liquid Nighttime 4oz plastic bottle

FDA recall notice · announced August 10, 2022 · The Procter & Gamble

Class II FDA/FSIS Class II: use may cause temporary or medically reversible adverse health consequences.

The product

Vicks Children's Botanicals Liquid Nighttime 4oz plastic bottle

Reason for recall

Acidified/Low Acid dietary supplement with no approved process.

Notes

Distribution: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, and West Virginia.
Lot/code information: 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
Quantity: 18,490 cases
Status: Terminated
Products in this recall event:
- Vicks ZzzQuil Liquid Melatonin Syrup Adult 8oz plastic bottle sold as single and twin pack (F-1537-2022)
- Vicks ZzzQuil Liquid Melatonin Syrup Pediatric 8oz plastic bottle sold as single and twin pack (F-1536-2022)
- Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles (F-1533-2022)
- Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle (F-1534-2022)
- Vicks Children's Botanicals Liquid Nighttime 4oz plastic bottle (F-1535-2022)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.