Recalls / Class I
Class IF-3369-2017
Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.
Product
Thymus Plus, No. 114, 90 Capsules, Dietary Supplement
- Type
- Food
- Affected lot / code info
- Lot 43701116, Exp 11/2019
- Quantity
- 107 bottles.
Why it was recalled
Undeclared allergens: milk (Colostrum)
Recalling firm
- Firm
- NatureAll-STF Holding, LLC
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 34 W Louise Ave, N/A, Salt Lake City, Utah 84115-3514
Distribution
- Distribution pattern
- Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.
Timeline
- Recall initiated
- 2017-07-26
- FDA classified
- 2017-08-14
- Posted by FDA
- 2017-08-23
- Terminated
- 2017-10-17
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-3369-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings.