The Procter & Gamble Company is recalling approximately 286,749 cases of Vicks Children's Botanicals Liquid and Vicks ZzzQuil Liquid Melatonin Syrup (both Adult and Pediatric formulas). These dietary supplements were manufactured without a validated process for low-acid products, which could lead to spoilage or the growth of harmful bacteria. The affected products were sold in 4oz and 8oz plastic bottles at retail stores nationwide. No injuries or illnesses have been reported to date.
The lack of an approved manufacturing process for low-acid dietary supplements can allow for microbial contamination or product spoilage. If consumed, contaminated products could cause illness, particularly in sensitive populations like children.
You have 2 options:
Quantity affected: 82,433 cases. Recall #: F-1533-2022.
Quantity affected: 34,526 cases. Recall #: F-1534-2022.
Quantity affected: 18,490 cases. Recall #: F-1535-2022.
Quantity affected: 60,778 cases. Recall #: F-1536-2022.
Quantity affected: 90,522 cases. Recall #: F-1537-2022.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES ยท Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.