FDA Food recall ·
Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving recall
This is an FDA Class I recall — the most serious type.
- Recall number
- F-0807-2025
- Date
- (initiated April 25, 2025)
- Company / brand
- My Life Inc
30315 Pacific Hwy S Ste F, Federal Way, WA, United States - Category
- Food › Class I
- Classification
- Class I
- Status
- Terminated
- Units affected
- 65 bottles in US and 62 bottles in South Korea
- Hazard tags
- Undeclared allergen
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG.
Why was it recalled?
Undeclared milk allergen
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
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
Sold to online consumers nationwide and distributed to Korea.
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (food), recall F-0807-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.