Recall · openFDA Food Enforcement

GnuPharma Relief 100% Herbal Supplement 60 Capsules: FDA Recall F-0297-2017

Agency action: May 8, 2017Record ID: F-0297-2017
View official source ↗

What happened

Original notice title

GnuPharma Relief 100% Herbal Supplement 60 Capsules, recall F-0297-2017

From the archived source record

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

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class II
Recall initiated by
Voluntary: Firm initiated
Report date
Jul 26, 2017
Termination date in the archive
Nov 15, 2018
Source checked
Jul 16, 2026
Record revision
eb5299bbcde0

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
GnuPharma Relief 100% Herbal Supplement 60 Capsules
Company
GnuPharma Corp.
Lot / identifier
products manufactured prior to May 8th, 2017.
Market / distribution
US