← FDA ENFORCEMENT
H-0907-2026Class I

The Coffee Connexion Co., Inc

Recalling firm
The Coffee Connexion Co., Inc
Product type
Food / supplement / cosmetic
Status
Ongoing
Report date
2026-06-10
Distribution
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
Firm state
TN
Product quantity
1) 1,553 cases; 2) 39 cases; 3) 3,063 cases
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination

Product description

1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0399549125016 2) Cheese Sauce Mix, 25 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954924308 3) Creamier Cheese Sauce Mix, 25 lb., packaged in a tied poly bag and packed 2 bags per case, UPC 0039954924483

Code / lot info

1) Cheese Sauce Mix, 25.5 oz.: Product Number: SSP071402 Batch: 045420 through 045424, Lot: 3495, Best By: 12/15/2027 Batch: 046194 through 046198, Lot: 0126, Best By: 01/12/2028 Batch: 047117 through 047120, Lot: 0406, Best By: 02/09/2028 Batch: 047950 through 047953, Lot: 0686, Best By: 03/09/2028 Batch: 049197 and 049200, Lot: 1176, Best By: 04/27/2028 2) Cheese Sauce Mix, 25 lb.: Product Number: SSP071530 Batch: 046520, Lot: 0266, Best By: 01/26/2028 Batch: 048386, Lot: 0826, Best By: 03/23/2028 Batch: 049227, Lot: 1176, Best By: 04/27/2028 3) Creamier Cheese Sauce Mix, 25 lb.: Product Number: SSP071550 Batch: 045307 through 045315 and 045317 through 045324, Lot: 3495, Best By: 12/15/2027 Batch: 046281 through 046297, Lot: 0196, Best By: 01/19/2028 Batch: 047201 through 047218, Lot: 0476, Best By: 02/16/2028 Batch: 048174 through 048192, Lot: 0756, Best By: 03/16/2028 Batch: 048906 through 048911 and 048913 through 048923, Lot: 1036, Best By: 04/13/2026

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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.