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F-1360-2024Class I

GRANDE CHEESE COMPANY

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
GRANDE CHEESE COMPANY
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2024-06-19
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.
Firm state
WI
Product quantity
1,726,910 lbs total
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Possible Salmonella contamination.

Product description

Grande Lactose SKU 30600. Grade A. Refined Pasteurized. Net Wt 25 kg. Ingredients: Lactose Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI

Code / lot info

Batch Number: ANS832-1, ANS832-2, ANS832-3, ANS832-4, ANS837-1, ANS837-2, ANS837-3, ANU961-1, ANU961-2, ANU961-3, ANU961-4, ANU961-5, ANU961-6, ANU961-7, ANV510-1, ANV510-2, ANV510-3, ANV510-4, ANV510-5, ANV510-6, ANV510-7, ANV516-1, ANV516-2, ANV516-3, ANV516-4, ANV516-5, ANV516-6, ANW439-4, ANW439-5, ANW439-6, ANW439-7, ANW439-8, ANW452-1, ANW452-2, ANW452-3, ANW452-4, ANW452-5, ANW452-6, ANW452-7, ANW459-5, ANW459-6, ANW459-7, ANW464-1, ANW464-2, ANW464-3, ANW464-4, ANW464-5, ANW464-6, ANY416-1, ANY416-2, ANY416-3, ANY416-4, ANY416-5, ANY416-6, ANY421-1, ANY421-2, ANY421-3, ANY421-4, ANY421-5, ANY421-6, ANY421-7, ANZ731-1, ANZ731-2, ANZ731-3, ANZ736-1, ANZ736-2, ANZ736-3, ANZ736-4, ANZ736-5, ANZ736-6, AOA588-1, AOA588-2, AOA588-3, AOA588-4, AOA588-5, AOA599-1, AOA599-2, AOA599-3 , AOA599-4, AOA599-5, AOA599-6, AOA776-1, AOA776-2, AOA776-3, AOA776-4, AOA776-5, AOA781-1, AOA781-2, AOA781-3 , AOA781-4, AOA781-5, AOA781-6, AOA793-1, AOA793-2, AOA793-3, AOA793-4, AOA793-5, AOC149-1, AOC149-2, AOC149-3, AOC149-4 , AOC149-5, AOC149-6, AOC491-1, AOC491-2, AOC491-3, AOC491-4, AOC491-5, AOC497-1, AOC497-2 , AOC497-3, AOC497-4, AOC497-5, AOC497-6, AOC600-1, AOC600-2, AOC600-3, AOC600-4, AOC600-5 , AOD986-1, AOD986-2, AOD986-3, AOD986-4 , AOD986-5, AOE006-1, AOE006-2, AOE006-3, AOE006-4 , AOE006-5, AOE006-6, AOE012-1, AOE012-2 , AOE012-3, AOE012-4, AOE012-5, AOE012-6, AOE012-7 , AOE012-8, AOE020-1, AOE020-2, AOE020-3 , AOE020-4, AOE020-5, AOE020-6, AOE025-1, AOE025-2 , AOE025-3, AOE025-4, AOE025-5, AOE025-6 , AOE032-1, AOE032-2, AOE032-3, AOE032-4, AOE032-5 , AOJ208-1, AOJ208-2, AOJ208-3, AOJ208-4 , AOJ208-5, AOJ208-6, AOJ208-7, AOJ628-1, AOJ628-2, AOJ628-3, AOK779-1, AOK779-2, AOK779-3 , AOK779-4, AOK779-5, AOK779-6, AOK809-1, AOK809-2, AOK809-3, AOK809-4, AOK809-5, AOK809-6 , AOK809-7, AOK816-1, AOK816-2, AOK816-3, AOK816-4, AOK816-5, AOL547-1, AOL547-2, AOL547-3 , AOL547-4, AOL547-5, AOL547-6, AOL581-3, AOL581-4.

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Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →