Important Recall: My Life Inc. Warns of Undeclared Milk in ML Natural Premium Quality Lactoferrin (Apolactoferrin)

Product Recall Issued for Lactoferrin Supplement

On April 25, 2025, My Life Inc., based in Federal Way, Washington, announced a recall of approximately 65 bottles of its product, ML Naturals Premium Quality Lactoferrin, marketed as Apolactoferrin 300mg capsules. This recall affects a specific lot, identified as lot number FL2407511L19, with an expiration date of October 2027. The reason for the recall is that the product may contain undeclared milk, posing a significant health risk for individuals with milk allergies.

Health Risks Associated with Undeclared Milk

The presence of undeclared milk in the Lactoferrin capsules is of particular concern for consumers who have an allergy or severe intolerance to milk. Exposure to milk proteins can lead to serious allergic reactions, including symptoms such as difficulty breathing, hives, swelling, gastrointestinal distress, or even anaphylaxis in extreme cases. Consumers who have purchased this product are urged to exercise caution, particularly those with known allergies.

Recommended Actions for Consumers

Consumers who are in possession of the affected lot of ML Naturals Premium Quality Lactoferrin are advised to refrain from using the product immediately. My Life Inc. recommends returning the product to the place of purchase for a full refund. Those with concerns or questions regarding the recall can contact the company directly for more information.

Importance of Product Recalls

Product recalls are crucial for maintaining public safety, as they protect consumers from potential health hazards associated with contaminated or mislabeled products. The U.S. Food and Drug Administration (FDA) plays a significant role in monitoring food and dietary supplements to ensure they meet safety standards. Recalls are initiated when unsafe products are identified, providing an opportunity for consumers to avoid health risks.

Reporting Adverse Effects

Consumers who experience adverse effects from using the recalled product are encouraged to report these issues to the FDA. This can be done through the FDA’s MedWatch program, which allows consumers to submit information about any health problems related to FDA-regulated products. Reporting such incidents helps the FDA track safety concerns and take actions to protect public health.

For more detailed information regarding the recall, consumers can visit the FDA’s official website here. It is essential for individuals to stay informed about recalls and safety alerts to ensure their health and well-being.

Source : www.fda.gov