Things sold in New York State have poison in them that can kill

A recent investigation has unveiled a critical health risk associated with dietary supplements sold by major retailers such as Amazon and Walmart in New York State. The U.S. Food and Drug Administration (FDA) has issued a warning regarding these products, revealing that they contain a dangerous poison capable of causing fatal outcomes.

The heart of this alarming issue is the detection of yellow oleander, a toxic plant native to Mexico and Central America, in certain over-the-counter diet pills. This discovery was made during routine inspections and tests conducted by the FDA, which led to the immediate flagging of these supplements due to their potential threat to consumer safety.

The ingestion of yellow oleander, even in small amounts, can lead to a wide range of critical health issues. The FDA has outlined the potential effects, which include severe neurological, gastrointestinal, and cardiovascular problems.

Individuals who consume the plant may experience symptoms such as nausea, vomiting, dizziness, diarrhea, and abdominal pain, which can escalate to more severe conditions like cardiac changes and dysrhythmias, potentially resulting in death.

The products implicated in this warning are identifiable by their association with the H&NATURAL brand and include:

  1. “Tejo Root” or “Raiz de Tejocte” under the H&Natural label, marketed as “Healthy and Natural.” These are 10g pills, available in boxes or bottles, with the specific UPC code: 196852946921.
  2. “Brazil Seed Pure Natural” or “Semilla de Brasil,” also under the H&Natural brand, presented as “Healthy and Natural.” These are seeds weighing 0.167g, packaged in boxes or bottles, identified by several UPC codes: 195893047529, 196852820641, 195893698721, 195893236893, 196852134618, and 195893336975.

These dietary supplements are currently under recall, especially those with expiration dates in March 2024 and May 2024. Consumers in possession of these items are strongly advised to discontinue their use immediately and consult with a healthcare professional if they have noticed any adverse effects after taking these products.

Additionally, the FDA urges consumers who have suffered adverse reactions or encountered quality issues with these dietary supplements to report their experiences to the MedWatch Adverse Event Reporting program. This initiative is crucial for the continuous monitoring and ensuring the safety of consumer products.

This incident underscores the critical need for consumers to exercise caution and perform due diligence when purchasing and consuming dietary supplements. Regulatory bodies like the FDA are pivotal in identifying and mitigating risks associated with consumer products, but awareness and proactive behavior from consumers are equally important in preventing health hazards.

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