My Life Inc food recall: Lactoferrin as Apolactoferrin 60 vegetarian capsules
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 96749
- Recall initiated
- Apr 25, 2025
- Classified by FDA
- May 20, 2025
- Posted in Enforcement Report
- May 28, 2025
- Terminated
- Jul 8, 2025
- Recalling firm
- My Life Inc
- Firm location
- Federal Way, WA, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Press Release
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Undeclared milk allergen
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Apr 25, 2025. FDA classified it 25 days later, on May 20, 2025. Distribution reported by FDA: Sold to online consumers nationwide and distributed to Korea.
Recalled products (1)
F-0807-2025 Class I Terminated
Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG.
Codes / lots: 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
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 96749
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.