DNPX Powder, 30 Blue Razz
Recalling firm: ProSupps USA LLC
Why it was recalled
Product contains the unapproved ingredient, picamilon.
The exact product
DNPX Powder, 30 Blue Razz
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
RLA106760915
Recall details
- Recall number
- F-3601-2017
- Event ID
- 78043
- FDA status
- Terminated
- Initiated
- Aug 30, 2017
- Reported
- Oct 11, 2017
- Classified
- Sep 29, 2017
- Terminated
- Feb 6, 2018
- Quantity
- 2 units
- Location
- Plano, TX, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
US and Canada
FDA source record · F-3601-2017
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.