Hyde V2 Berry Blast
Recalling firm: ProSupps USA LLC
Why it was recalled
Product contains the unapproved ingredient, picamilon.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 6, 2018.
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ProductHyde V2 Berry Blast
FDA code information
A109121215, XA102900615
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Full FDA record and distribution details
Original product description
Hyde V2 Berry Blast
Original FDA recall reason
Product contains the unapproved ingredient, picamilon.
Recall details
- Recall number
- F-3595-2017
- Event ID
- 78043
- FDA status
- Terminated
- Initiated
- Aug 30, 2017
- Reported
- Oct 11, 2017
- Classified
- Sep 29, 2017
- Terminated
- Feb 6, 2018
- Quantity
- 3803 units
- Location
- Plano, TX, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
US and Canada
FDA source record · F-3595-2017
Data updated September 16, 2026. View official FDA data ↗
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