Class ITerminatedVoluntary: Firm initiated
My Life Inc: food recall F-0807-2025
My Life Inc of Federal Way, WA recalled Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG. Reason: Undeclared milk allergen. The FDA listed it as Class I in its Enforcement Report dated May 28, 2025; distribution: nationwide.
Record status as published: Terminated (terminated Jul 8, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG.
- Product quantity
- 65 bottles in US and 62 bottles in South Korea
- Reason for recall
- Undeclared milk allergen
- Codes, lots and dates on the package
- 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.
- Distribution pattern
- Sold to online consumers nationwide and distributed to Korea.
- Recalling firm
- My Life Inc, Federal Way, WA
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Press Release
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Apr 25, 2025 |
| Classified by the FDA | May 20, 2025 |
| Published in the Enforcement Report | May 28, 2025 |
| Terminated | Jul 8, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0807-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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