Aramark Cheese Sauce New & Improved, 25 lb., packaged in a tied poly bag and packed 2 bags per case, UPC 0039954925121
Summary
The FDA issued a Class I for Aramark Cheese Sauce New & Improved, 25 lb., packaged in a tied poly bag and pac 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-0908-2026
Action Date
2026-06-10
Status
Ongoing
Category
food
Product Description
Aramark Cheese Sauce New & Improved, 25 lb., packaged in a tied poly bag and packed 2 bags per case, UPC 0039954925121
Lot/Code Info: Product Number: SSP071425 Batch: 045542 through 045550 and 045552 through 045570, Lot: 3565, Best By: 12/22/2027 Batch: 045832 through 045871, Lot: 0056, Best By: 01/05/2028 Batch: 046298 through 046337, Lot: 0196, Best By: 01/19/2028 Batch: 047031 through 047065, Lot: 0406, Best By: 02/09/2028 Batch: 047307 through 047341, Lot: 0546, Best By: 02/23/2028 Batch: 047865 through 047901, Lot: 0686, Best By: 03/09/2028 Batch: 048276 through 048312, Lot: 0826, Best By: 03/23/2028 Batch: 048705 through 048736, Lot: 0966, Best By: 04/06/2028 Batch: 048953 through 048984, Lot: 1106, Best By: 04/20/2028
Quantity Affected: 10,958 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-0908-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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