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Grande Ultra 9100 Functional Whey Protein Isolate. SKU 32131. 90% Protein. Grade A. Pasteurized. Net Wt 20 kg. Ingredients: Whey Protein Isolate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI

Class I - Dangerous
Recalled: May 1, 2024 GRANDE CHEESE COMPANY Dairy & Eggs Nationwide

What Should You Do?

  1. Check if you have this product:
    Batch Numbers: ANU825-1, ANU825-2, ANU825-3, ANU825-4, ANU956-1, ANU956-2, ANU956-3, ANU956-4, ANW450-1, ANW450-2, ANW450-3, ANW450-4, ANW462-1, ANW462-2, ANW462-3, ANW462-4, ANX889-1, ANX889-2, ANX889-3 , ANX889-4, ANY419-1, ANY419-2, ANY419-3, ANY419-4, ANZ341-1, ANZ341-2, ANZ341-3, ANZ734-1 , ANZ734-2, ANZ734-3, ANZ734-4, AOA597-1, AOA597-2, AOA597-3, AOI521-1, AOI521-2, AOJ157-1 , AOJ157-2, AOJ157-3, AOJ206-1, AOJ206-2, AOJ206-3, AOK807-1, AOK807-2, AOK807-3, AOL545-1 , AOL584-1, AOL584-2, AOL584-3, AON172-1, AON172-2, AON172-3.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
GRANDE CHEESE COMPANY
Reason for Recall:
Possible Salmonella contamination.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Grande Ultra 9100 Functional Whey Protein Isolate. SKU 32131. 90% Protein. Grade A. Pasteurized. Net Wt 20 kg. Ingredients: Whey Protein Isolate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI

Product Codes/Lot Numbers:

Batch Numbers: ANU825-1, ANU825-2, ANU825-3, ANU825-4, ANU956-1, ANU956-2, ANU956-3, ANU956-4, ANW450-1, ANW450-2, ANW450-3, ANW450-4, ANW462-1, ANW462-2, ANW462-3, ANW462-4, ANX889-1, ANX889-2, ANX889-3 , ANX889-4, ANY419-1, ANY419-2, ANY419-3, ANY419-4, ANZ341-1, ANZ341-2, ANZ341-3, ANZ734-1 , ANZ734-2, ANZ734-3, ANZ734-4, AOA597-1, AOA597-2, AOA597-3, AOI521-1, AOI521-2, AOJ157-1 , AOJ157-2, AOJ157-3, AOJ206-1, AOJ206-2, AOJ206-3, AOK807-1, AOK807-2, AOK807-3, AOL545-1 , AOL584-1, AOL584-2, AOL584-3, AON172-1, AON172-2, AON172-3.

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1367-2024

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