Food recall

My Life Inc recall: Lactoferrin as Apolactoferrin 60 vegetarian capsules

My Life Inc, of Federal Way, WA, recalled Lactoferrin as Apolactoferrin 60 vegetarian capsules. The FDA's reason: “Undeclared milk allergen.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on April 25, 2025, and the FDA first listed it in its Enforcement Report of May 28, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class I

It could cause serious harm or death

Why

Allergen not on the label

Status

Terminated

Closed July 8, 2025

The recall

Company
My Life Inc (Federal Way, WA)
Reason, in FDA's words
“Undeclared milk allergen”
Where it was sold
Sold to online consumers nationwide and distributed to Korea.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
96749

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0807-2025 Class I

    Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG.

    Codes: Lot #FL2407511L19 Batch #FL2407511 Expire By/Expiration date 10/2027 Batch #FL2407511 is the CoA Batch Number from supplier and L19 is the recalling firm's internal code for Lactoferrin.

    Quantity: 65 bottles in US and 62 bottles in South Korea

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of May 28, 2025.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.