Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving.
Recalling firm: My Life Inc
Why it was recalled
Undeclared milk allergen
The exact product
Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG.
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original 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.
| Type | Code / value | Context |
|---|---|---|
| UPC | 850062613157 | Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG. |
| batch | FL2407511 | Lot #FL2407511L19 Batch #FL2407511 Expire By/Expiration date 10/2027 Batch #FL2407511 is the CoA Batch Number from supplier and L19 is the recalling fir |
| batch | FL2407511 | 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. |
| lot | FL2407511L19 | Lot #FL2407511L19 Batch #FL2407511 Expire By/Expiration date 10/2027 Batch #FL2407511 is the CoA Batch Number from supplier and L19 is |
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 ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.