Walmart Inc is recalling approximately 1,308 bottles of Artri King and Artri Ajo King tablets because they were found to contain diclofenac, a prescription-strength anti-inflammatory drug (NSAID) that is not listed on the label. The products were also marketed with unapproved drug claims about treating pain and inflammation. While no injuries have been reported, these tablets were sold nationwide at Walmart locations and online.
Undeclared diclofenac can cause serious side effects, including gastrointestinal bleeding, heart attack, or stroke, especially if taken with other NSAIDs or by people with certain health conditions. Because the medication is not listed on the label, consumers may accidentally take dangerous amounts of this drug without medical supervision.
You have 2 options:
Quantity: 1,308 bottles total across items
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.