Class IITerminated in FDA datasetMay 8, 2017

GnuPharma ECS Herbal Tea Relief SAMPLE ONLY

Recalling firm: GnuPharma Corp.

Why it was recalled

1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)

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ProductGnuPharma ECS Herbal Tea Relief SAMPLE ONLY

FDA code information

products manufactured prior to May 8th, 2017.

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Full FDA record and distribution details

Original product description

GnuPharma ECS Herbal Tea Relief SAMPLE ONLY

Recall details

Recall number
F-0301-2017
Event ID
77506
FDA status
Terminated
Initiated
May 8, 2017
Reported
Jul 26, 2017
Classified
Jul 18, 2017
Terminated
Nov 15, 2018
Quantity
1 unit (4 tablespoons)
Location
Owasso, OK, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

US

FDA source record · F-0301-2017

Data updated September 16, 2026. View official FDA data ↗

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