Recalls / Class II
Class IIF-3591-2017
Product
Dr. Jekyll V2 Orange Burst Domestic 30; Dr. Jekyll Orange Burst domestic sample packs
- Type
- Food
- Affected lot / code info
- A107911115, A110400216, X016652L1
- Quantity
- 65,195 units
Why it was recalled
Product contains the unapproved ingredient, picamilon.
Recalling firm
- Firm
- ProSupps USA LLC
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 2801 E Plano Pkwy, N/A, Plano, Texas 75074-7418
Distribution
- Distribution pattern
- US and Canada
Timeline
- Recall initiated
- 2017-08-30
- FDA classified
- 2017-09-29
- Posted by FDA
- 2017-10-11
- Terminated
- 2018-02-06
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-3591-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings.