GnuPharma Relief 100% Herbal Supplement 60 Capsules recall

Recalled by GnuPharma Corp. · Owasso, OK, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

Shiga toxin-producing E. coli (such as O157:H7) can cause severe illness and kidney failure.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

GnuPharma Relief 100% Herbal Supplement 60 Capsules

Quantity: 244 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

products manufactured prior to May 8th, 2017.

Where it was sold

FDA's distribution note: US

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: GnuPharma Corp.
Initiated by: Voluntary: Firm initiated
Recall initiated: May 8, 2017
In FDA report of: Jul 26, 2017
Terminated: Nov 15, 2018
FDA recall number: F-0297-2017 · event 77506
Official record: FDA enforcement report search

Also recalled with it (5 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated E. coli May 8, 2017