My Diary Bromelain Recall Due to Milk Allergen

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KFDA Issues Recall of MyDay Bromelain Due to Undeclared Milk Allergen

KFDA Issues Recall of MyDay Bromelain Due to Undeclared Milk Allergen

The Korea Food and Drug Administration (KFDA) has ordered the recall of the dietary supplement “MyDay Bromelain” after discovering it contains undeclared milk allergens, according to a report by Seoul-based news outlet News1. The product, marketed for digestive health, poses a risk to individuals with milk allergies.

Details of the Recall

The KFDA identified that “MyDay Bromelain,” produced by an unspecified manufacturer, included milk-derived ingredients without proper labeling. The agency emphasized that such omissions violate food safety regulations, as milk is a common allergen requiring explicit disclosure. The recall applies to all batches of the product distributed in South Korea.

Details of the Recall

What Consumers Should Do

Consumers who have purchased “MyDay Bromelain” are advised to stop using the product immediately. The KFDA recommends contacting the manufacturer for refunds or disposal instructions. Individuals experiencing allergic reactions should seek medical attention and report the issue to the agency. The recall notice includes a list of affected batch numbers and expiration dates, which are detailed in the News1 report.

Implications for Allergen Labeling

This incident highlights the critical importance of accurate ingredient labeling in dietary supplements. Milk allergies can cause severe reactions, including anaphylaxis, making transparency essential. The KFDA has reiterated its commitment to enforcing strict labeling protocols to prevent similar cases, stating that “consumer safety remains the top priority.”

Recall Roundup for Feb. 16, 2026

Industry Response and Precautions

While the manufacturer has not yet issued a public statement, the KFDA has initiated an investigation into the production process. Industry experts warn that such recalls underscore the need for rigorous quality control in supplement manufacturing. Consumers are encouraged to verify product labels and consult healthcare providers before using new supplements.

The KFDA’s action aligns with global trends toward stricter allergen management,

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