ProSupps USA LLC recalls Dr. Jekyll V2 Orange Burst Domestic 30; Dr. Jekyll Orange Burst domestic sample packs
- Recall date
- August 30, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- F-3591-2017
- FDA classification
- Class II
- Brand / firm
- ProSupps USA LLC
- Sold / distributed
- US and Canada
Why it was recalled
Product contains the unapproved ingredient, picamilon.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Dr. Jekyll V2 Orange Burst Domestic 30; Dr. Jekyll Orange Burst domestic sample packs
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