RecallHawk
Class I Recall

Grande Ultra 9150 Whey Protein Isolate. Product Code: 32324. 90% Protein. Grade A. Pasteurized. Net Wt 20 kg. Ing

GRANDE CHEESE COMPANY

Summary

The FDA issued a Class I for Grande Ultra 9150 Whey Protein Isolate. Product Code: 32324. 90% Protein. Gr by GRANDE CHEESE COMPANY. Reason: Possible Salmonella contamination..

Details

Source

Food Recall

External ID

F-1369-2024

Action Date

2024-06-19

Status

Terminated

Category

food

Product Description

Grande Ultra 9150 Whey Protein Isolate. Product Code: 32324. 90% Protein. Grade A. Pasteurized. Net Wt 20 kg. Ingredients: Whey Protein Isolate Contains Milk. Manufactured By: Grande Custom Ingredients Group, 1007 West Lake Street, Friendship, WI 53934.

Lot/Code Info: Batch Numbers: ANU031-1, ANU031-2, ANU031-3, AOB114-1, AOB114-2, AOB114-3, AOC147-1, AOC147-2, AOC147-3, AOC495-1, AOC495-2, AOC495-3, AOD984-1, AOD984-2, AOD984-3, AOE010-1, AOE010-2, AOE023-1.

Quantity Affected: 1,726,910 lbs total

Reason for Recall

Possible Salmonella contamination.

Distribution

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.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-05-01

Company

GRANDE CHEESE COMPANY

Fond Du Lac, WI

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 88 food recalls issued in the same week, part of 204 food-related FDA actions this month.

GRANDE CHEESE COMPANY has 11 FDA actions in our database, including 11 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (GRANDE CHEESE COMPANY) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does GRANDE CHEESE COMPANY have FDA actions?

GRANDE CHEESE COMPANY has 11 FDA actions in our database, including 11 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1369-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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