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Class I: FDA’s highest-risk recall class
Ongoing means the FDA still lists this recall as open — not that every package is affected.
Source: U.S. Food and Drug Administration · Reported June 10, 2026 · Not a government service
From the FDA record
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
How to check
Select the package that matches what you have, then check the details on yours against this recall.
Package size: 25.5 oz · 25 lb
Recall lists UPC 03995491250162
Recall lists lot / batch: 045420; 3495; 046194; 0126; 047117; 0406; 047950; 0686; 049197; 1176; 046520; 0266; 048386; 0826; 049227; 045307; 046281; 0196; 047201; 0476; 048174; 0756; 048906; 1036
Recall lists best-by / use-by: 2027-12-15 to 2027-12-15; 2028-01-12 to 2028-01-12; 2028-02-09 to 2028-02-09; 2028-03-09 to 2028-03-09; 2028-04-27 to 2028-04-27; 2028-01-26 to 2028-01-26; 2028-03-23 to 2028-03-23; 2028-01-19 to 2028-01-19; 2028-02-16 to 2028-02-16; 2028-03-16 to 2028-03-16; 2026-04-13 to 2026-04-13
Package size: 3 lb · 7 oz
Recall lists UPC 0039954921963
Recall lists lot / batch: 046188; 0126; 047290; 0476; 048029; 0686; 049089; 1106
Recall lists best-by / use-by: 2028-01-12 to 2028-01-12; 2028-02-16 to 2028-02-16; 2028-03-09 to 2028-03-09; 2028-04-20 to 2028-04-20
Package size: 25 lb
Recall lists UPC 0039954925121
Recall lists lot / batch: 045542; 3565; 045832; 0056; 046298; 0196; 047031; 0406; 047307; 0546; 047865; 0686; 048276; 0826; 048705; 0966; 048953; 1106
Recall lists best-by / use-by: 2027-12-22 to 2027-12-22; 2028-01-05 to 2028-01-05; 2028-01-19 to 2028-01-19; 2028-02-09 to 2028-02-09; 2028-02-23 to 2028-02-23; 2028-03-09 to 2028-03-09; 2028-03-23 to 2028-03-23; 2028-04-06 to 2028-04-06; 2028-04-20 to 2028-04-20
Site guidance
Check your package against the affected product information below. The FDA enforcement record does not include product-specific return or disposal instructions. Review the official notice or contact the recalling company before taking action.
From the FDA record
AL, AR, AZ, CA, CO, FL, GA, IL, IN, IA, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WY
Distribution information reflects what was reported in the FDA record and may not include every downstream location.
Class I
FDA’s highest-risk recall class