Check the Batch
Class ITerminated in FDA datasetRecall initiated Apr 25, 2025

Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving.

Recalling firm: My Life Inc

Why it was recalled

Undeclared milk allergen

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 8, 2025.

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Compare the exact product and package details with the label you have.

ProductLactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG.
UPC850062613157

FDA code information

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.

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC850062613157Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG.
batchFL2407511Lot #FL2407511L19 Batch #FL2407511 Expire By/Expiration date 10/2027 Batch #FL2407511 is the CoA Batch Number from supplier and L19 is the recalling fir
batchFL2407511Lot #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.
lotFL2407511L19Lot #FL2407511L19 Batch #FL2407511 Expire By/Expiration date 10/2027 Batch #FL2407511 is the CoA Batch Number from supplier and L19 is

Original FDA recall reason

Undeclared milk allergen

Recall details

Recall number
F-0807-2025
Event ID
96749
FDA status
Terminated
Initiated
Apr 25, 2025
Reported
May 28, 2025
Classified
May 20, 2025
Terminated
Jul 8, 2025
Quantity
65 bottles in US and 62 bottles in South Korea
Location
Federal Way, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Sold to online consumers nationwide and distributed to Korea.

FDA source record · F-0807-2025

Data updated September 16, 2026. View official FDA data ↗

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