Grande Bravo 600 Functional Whey Protein recall

Recalled by Grande Cheese Company · Fond Du Lac, WI, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Possible Salmonella contamination.

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

Grande Bravo 600 Functional Whey Protein SKU 32106. 34% Protein. Grade A. Pasteurized. Net Wt 50 lbs. Ingredients: Whey Protein Concentrate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI

Quantity: 1,726,910 lbs total

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.

Batch Numbers: AMV955-1, AMV955-2, ANU045-1, ANU045-2, ANU837-1.

Where it was sold

Arkansas California Colorado Georgia Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Michigan Minnesota Missouri North Carolina New Jersey New York Ohio Pennsylvania South Dakota Tennessee Texas Utah Wisconsin

FDA's distribution note: AR, CA, CO, GA, ID, IL, IN, KS, KY, LA, MA, MI, MN, MO, NC, NJ, NY, OH, PA, SD, TN, TX, UT, WI. Outside the US to Canada, Ecuador, and Japan.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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: Grande Cheese Company
Initiated by: Voluntary: Firm initiated
Recall initiated: May 1, 2024
In FDA report of: Jun 19, 2024
Terminated: Jun 26, 2025
FDA recall number: F-1366-2024 · event 94540
Official record: FDA enforcement report search

Also recalled with it (10 more products)

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

Class I · High risk Terminated Salmonella May 1, 2024