Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and pack…
Recalled by The Coffee Connexion Co., Inc
Food recall
The Coffee Connexion Co., Inc
Class I — most serious
There is a reasonable chance that using this product could cause serious health problems or death.
The Coffee Connexion Co., Inc has recalled Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and pack…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on June 10, 2026 and was initiated on May 6, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and pack…, with approximately 1,675 cases affected. The company behind the recall is The Coffee Connexion Co., Inc, based in Lebanon, TN. The FDA describes the product as: “Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458”
Why was Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and pack… recalled?
According to the FDA, the stated reason for the recall is: “Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination.” In plain terms, this recall relates to Salmonella.
Salmonella is a group of bacteria that is one of the most common causes of foodborne illness in the United States. Public health authorities note that infections can lead to symptoms such as fever, diarrhea, and stomach cramps, and that young children, older adults, and people with weakened immune systems are at higher risk of serious illness. Because it can spread through contaminated food, regulators treat Salmonella findings seriously.
What should you do?
If you think you may have bought Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and pack…, compare it against the product description and identifying codes (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: 0482…) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact The Coffee Connexion Co., Inc or your local health authority.
About this recall
This recall was distributed in TN. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Ongoing
- Date reported
- June 10, 2026
- Recall started
- May 6, 2026
- Distributed in
- TN
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and pack… recalled?+
According to the FDA: Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella…
How serious is this recall?+
Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.
What should I do if I have Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and pack…?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0910-2026. Information last synced from the FDA on July 5, 2026.