Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458
Summary
The FDA issued a Class I for Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per by The Coffee Connexion Co., Inc. Reason: Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination.
Details
Source
Food Recall
External ID
H-0910-2026
Action Date
2026-06-10
Status
Ongoing
Category
food
Product Description
Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458
Lot/Code Info: 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
Quantity Affected: 1,675 cases
Reason for Recall
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
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
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-06
Company
Lebanon, TN
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 166 food recalls issued in the same week, part of 204 food-related FDA actions this month.
The Coffee Connexion Co., Inc has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (The Coffee Connexion Co., Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The Coffee Connexion Co., Inc have FDA actions?
The Coffee Connexion Co., Inc has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0910-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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