Aramark Cheese Sauce New & Improved recall
Recalled by The Coffee Connexion Co., Inc
The product, as the FDA describes it: Aramark Cheese Sauce New & Improved, 25 lb., packaged in a tied poly bag and packed 2 bags per case, UPC 0039954925121
Why it was recalled
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
What to do if you have it
Nothing about aramark cheese sauce new & improved will look or smell wrong, because the organisms behind this kind of recall leave no trace you can see or taste. Do not cook it to make it safe and do not sample it. Throw it out or return it, then wash anything it touched, including the shelf it sat on and the container beside it.
How to tell whether your package is one of them
A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.
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
The details on record
| Recalling company | The Coffee Connexion Co., Inc |
|---|---|
| Company location | Lebanon, TN |
| 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 |
| How much was recalled | 10,958 cases |
| Recall started | May 6, 2026 |
| Published by the FDA | June 10, 2026 |
| Recall type | Voluntary: Firm initiated |
| How the company announced it | Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit |
| FDA recall number | H-0908-2026 |
Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.
The other half of the answer
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