Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG.
Summary
The FDA issued a Class I for Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 by My Life Inc. Reason: Undeclared milk allergen.
Details
Source
Food Recall
External ID
F-0807-2025
Action Date
2025-05-28
Status
Terminated
Category
food
Product Description
Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG.
Lot/Code Info: 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 Affected: 65 bottles in US and 62 bottles in South Korea
Reason for Recall
Undeclared milk allergen
Distribution
Sold to online consumers nationwide and distributed to Korea.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-25
Company
Federal Way, WA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (My Life Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does My Life Inc have FDA actions?
This is the only FDA action we have on record for My Life Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0807-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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