Why it was recalled
Product is potentially mislabeled and contains the non-dietary ingredient Picamilon.
Product description
Dr. Jekyll V2 Orange Burst domestic
Lot numbers, UPCs & expiration codes
A109850116
Where it was sold
US and Canada
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-2408-2017
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- May 16, 2017
- FDA report date
- Jul 5, 2017
- Quantity
- 698 units
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- ProSupps USA LLC
Original FDA data
Every field from FDA enforcement report F-2408-2017, exactly as published.
Show all FDA fields
- City
- Plano
- State
- TX
- Status
- Terminated
- Country
- United States
- Event ID
- 77285
- Address
- 2801 E Plano Pkwy
- Code information
- A109850116
- Postal code
- 75074-7418
- Report date
- Jul 5, 2017
- Product type
- Food
- Recall number
- F-2408-2017
- Classification
- Class II
- Recalling firm
- ProSupps USA LLC
- Product quantity
- 698 units
- Termination date
- Feb 6, 2018
- Reason for recall
- Product is potentially mislabeled and contains the non-dietary ingredient Picamilon.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Dr. Jekyll V2 Orange Burst domestic
- Distribution pattern
- US and Canada
- Recall initiation date
- May 16, 2017
- Initial firm notification
- Letter
- Center classification date
- Jun 28, 2017