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FDAClass I · Food · Recalled June 10, 2026

1) Cheese Sauce Mix recall — The Coffee Connexion Co., Inc

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

Class I: most serious — reasonable probability of serious health consequences or death.

View the official FDA enforcement record (openFDA) ↗

Official recall ID
H-0907-2026
Brand
The Coffee Connexion Co
Classification
Class I
Units affected
1) 1,553 cases; 2) 39 cases; 3) 3,063 cases
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

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

Affected products

Companies & origin

Recalling firm location
Lebanon, TN, United States
Firm address
216 E Main St, 37087-2826

Identifying details (verbatim from the notice)

Product codes / lots
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
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 notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
98925
Recall initiated
May 6, 2026
FDA classified
June 4, 2026
FDA report date
June 10, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.

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