F-1360-2024Class I

GRANDE CHEESE COMPANY

Recalling firm

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

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 openFDA enforcement API. 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.