Check the Batch
Class ICompleted in FDA datasetRecall initiated May 6, 2026

Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case

Recalling firm: The Coffee Connexion Co., Inc

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Completed” describes the FDA recall process; it does not certify that an individual package is safe.

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Compare the exact product and package details with the label you have.

ProductCold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458
Package size20 lb

FDA code information

Product Number: SSP980720 Batch: 046390 through 046393, Lot: 0196, Best By: 01/19/2028 Batch: 047107 through 047112, Lot: 0406, Best By: 02/09/2028 Batch: 048236 through 048239, Lot: 0756, Best By: 03/16/2028 Batch: 048762 through 048766, Lot: 0966, Best By: 04/06/2028 Batch: 049018 through 049022, Lot: 1106, Best By: 04/20/2028 Batch: 049218 through 049222, Lot: 1176, Best By: 04/27/2028

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458

Extracted codes and context

TypeCode / valueContext
best by01/19/2028Product Number: SSP980720 Batch: 046390 through 046393, Lot: 0196, Best By: 01/19/2028 Batch: 047107 through 047112, Lot: 0406, Best By: 02/09/2028 Batch: 048236 through 048239, Lot: 0756, Best By: 03/16/20
best by02/09/2028ot: 0196, Best By: 01/19/2028 Batch: 047107 through 047112, Lot: 0406, Best By: 02/09/2028 Batch: 048236 through 048239, Lot: 0756, Best By: 03/16/2028 Batch: 048762 through 048766, Lot: 0966, Best By: 04/06/20
best by03/16/2028ot: 0406, Best By: 02/09/2028 Batch: 048236 through 048239, Lot: 0756, Best By: 03/16/2028 Batch: 048762 through 048766, Lot: 0966, Best By: 04/06/2028 Batch: 049018 through 049022, Lot: 1106, Best By: 04/20/20
best by04/06/2028ot: 0756, Best By: 03/16/2028 Batch: 048762 through 048766, Lot: 0966, Best By: 04/06/2028 Batch: 049018 through 049022, Lot: 1106, Best By: 04/20/2028 Batch: 049218 through 049222, Lot: 1176, Best By: 04/27/20
best by04/20/2028ot: 0966, Best By: 04/06/2028 Batch: 049018 through 049022, Lot: 1106, Best By: 04/20/2028 Batch: 049218 through 049222, Lot: 1176, Best By: 04/27/2028
best by04/27/2028ot: 1106, Best By: 04/20/2028 Batch: 049218 through 049222, Lot: 1176, Best By: 04/27/2028
lot0196Product Number: SSP980720 Batch: 046390 through 046393, Lot: 0196, Best By: 01/19/2028 Batch: 047107 through 047112, Lot: 0406, Best By: 02/09/2028 Batch: 048236 through 048239, Lot: 07
lot0406rough 046393, Lot: 0196, Best By: 01/19/2028 Batch: 047107 through 047112, Lot: 0406, Best By: 02/09/2028 Batch: 048236 through 048239, Lot: 0756, Best By: 03/16/2028 Batch: 048762 through 048766, Lot: 09
lot0756rough 047112, Lot: 0406, Best By: 02/09/2028 Batch: 048236 through 048239, Lot: 0756, Best By: 03/16/2028 Batch: 048762 through 048766, Lot: 0966, Best By: 04/06/2028 Batch: 049018 through 049022, Lot: 11
lot0966rough 048239, Lot: 0756, Best By: 03/16/2028 Batch: 048762 through 048766, Lot: 0966, Best By: 04/06/2028 Batch: 049018 through 049022, Lot: 1106, Best By: 04/20/2028 Batch: 049218 through 049222, Lot: 11
lot1106rough 048766, Lot: 0966, Best By: 04/06/2028 Batch: 049018 through 049022, Lot: 1106, Best By: 04/20/2028 Batch: 049218 through 049222, Lot: 1176, Best By: 04/27/2028
lot1176rough 049022, Lot: 1106, Best By: 04/20/2028 Batch: 049218 through 049222, Lot: 1176, Best By: 04/27/2028

Original FDA recall reason

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

Recall details

Recall number
H-0910-2026
Event ID
98925
FDA status
Completed
Initiated
May 6, 2026
Reported
Jun 10, 2026
Classified
Jun 4, 2026
Quantity
1,675 cases
Location
Lebanon, TN, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

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

FDA source record · H-0910-2026

Data updated September 16, 2026. View official FDA data ↗

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