MODERATE RISK
Terminated
F-0298-2017
GnuPharma Sleep 100% Herbal Supplement 60 Capsules
Recalled by GnuPharma Corp.
Classification
Class II — Products that might cause a temporary health problem, or pose only a slight threat of a serious nature.
Reason for Recall
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Product Details
Product Quantity
1 bottle
Product Type
Food
Code Info
products manufactured prior to May 8th, 2017.
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
US
Company Location
Owasso, OK, 74055-2098
Timeline
Report Date
07/26/2017
Recall Initiated
05/08/2017
Classification Date
07/18/2017
Termination Date
11/15/2018
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 28, 2026
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