Urgent Recall: Dorado Nutrition’s Spermidine 10mg Capsules Contain Undeclared Wheat Allergen

Product Recall Issued For Spermidine Maximum Strength

Supplement Manufacturing Partners, Inc. is initiating a recall of its Dorado Nutrition brand Spermidine Maximum Strength 10 MG per serving due to an undeclared wheat allergen. The presence of wheat poses significant health risks for individuals with allergies or severe sensitivities to wheat, potentially leading to serious or life-threatening allergic reactions.

Reason For Recall

The recall was prompted after it was discovered that the product contained wheat, which was not listed on the ingredient label. This oversight puts consumers who may be allergic to wheat at risk, highlighting the critical need for transparency and accuracy in dietary supplement labeling.

Health Risks

For those with wheat allergies or sensitivities, consuming Dorado Nutrition Spermidine Maximum Strength could trigger severe allergic reactions. Symptoms of a wheat allergy can range from gastrointestinal distress to more severe reactions such as anaphylaxis, which can be life-threatening. The recall serves as a vital precaution to prevent potential health emergencies among at-risk individuals.

Recommended Actions For Consumers

Consumers who have purchased the affected product are advised to stop using it immediately. They should return the product to the place of purchase for a full refund. Supplement Manufacturing Partners, Inc. is actively working to ensure that consumers are informed about this recall and to facilitate an easy return process.

Importance Of Product Recalls

Product recalls play a crucial role in public safety, ensuring that potentially harmful products are removed from the market and consumers are alerted to potential risks. The FDA monitors these recalls to protect consumers and maintain trust in the safety of dietary supplements.

Reporting Adverse Effects

Consumers who experience any adverse effects related to the consumption of the recalled product are encouraged to report these incidents to the FDA. Reports can be submitted through the FDA’s MedWatch program, which provides a mechanism for consumers and healthcare professionals to share information about product-related health issues.

For more detailed information about the recall, individuals can visit the FDA’s official website at www.fda.gov.

Source : www.fda.gov