Recall Register

Food recall: GnuPharma Fit 100% Herbal Supplement 60 Capsules

Class II FDA enforcement event 77506. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

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

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

GnuPharma Corp. started this food recall on 8 May 2017. The firm address in the FDA record is in Owasso, OK. FDA put the recall in Class II. FDA event 77506 has 6 product records. The first FDA enforcement report date is 26 Jul 2017. The record gives the status Terminated, with the termination date 15 Nov 2018.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

US

Recalling firm

GnuPharma Corp., Owasso, OK.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

6 product records in the event.

FDA event 77506: product records
Recall numberProductQuantityClassStatusReport date
F-0296-2017GnuPharma Fit 100% Herbal Supplement 60 Capsules56 bottlesClass IITerminated26 Jul 2017
F-0297-2017GnuPharma Relief 100% Herbal Supplement 60 Capsules244 bottlesClass IITerminated26 Jul 2017
F-0298-2017GnuPharma Sleep 100% Herbal Supplement 60 Capsules1 bottleClass IITerminated26 Jul 2017
F-0299-2017GnuPharma Stress 100% Herbal Supplement 60 Capsules131 bottlesClass IITerminated26 Jul 2017
F-0300-2017GnuPharma Foundation 100% Herbal Supplement 60 Capsules9 bottlesClass IITerminated26 Jul 2017
F-0301-2017GnuPharma ECS Herbal Tea Relief SAMPLE ONLY1 unit (4 tablespoons)Class IITerminated26 Jul 2017

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Food events that started in 2017
599
Share of these events in Class II
52%
Product records in this event
6
Events of the firm on the register
1

Official channels

Cite this page

Recall Register. FDA enforcement event 77506. https://recallregister.com/fda/ii/77506/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: US
What quantity of product is in FDA event 77506?
The event has 6 product records. The first record gives this quantity: 56 bottles
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2017 have the same class?
52% of the 599 food events that started in 2017 are in Class II.