Food Recall Check
Class II · Moderate risk Terminated Initiated May 23, 2013 (13 years ago)

Mother Earth Products recall

Recalled by Mother Earth International LLC · Ames, IA, United States

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

Why it was recalled

The product was manufactured with a Soy Protein Isolate manufactured by CHS, Inc and may be contaminated with Salmonella.

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

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

Mother Earth Products, Veggie Burger, Textured Vegetable Protein, packaged in 2-cup mylar bags, 1-quart mylar bags, 1-quart plastic jar, 1-gallon mylar bags, 5-lb mylar bags, 15-lb bulk bag, 25-lb bulk box and TVP Variety Sample Pack.

Quantity: 210 lbs.

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.

They use a manufacture date code. 712 means July 2012. Their customer letter states product manufactured July 1, 2012 to present.

Where it was sold

Nationwide.

FDA's distribution note: Distribution was nationwide through internet sales. No foriegn or military distribution was made.

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
Mother Earth International LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
May 23, 2013
In FDA report of
Jul 17, 2013
Terminated
Jan 22, 2014
FDA recall number
F-1590-2013 · event 65262
Official record
FDA enforcement report search