The Coffee Connexion Co., Inc Recall: Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination

🇺🇸 United States

1. May 6, 2026 - Recall initiated
2. June 10, 2026 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-0907-2026

Event ID

98925

Status

Ongoing

Classification

Class I

Company

The Coffee Connexion Co., Inc

Product description

1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0399549125016 2) Cheese Sauce Mix, 25 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954924308 3) Creamier Cheese Sauce Mix, 25 lb., packaged in a tied poly bag and packed 2 bags per case, UPC 0039954924483

Quantity

1) 1,553 cases; 2) 39 cases; 3) 3,063 cases

Reason

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

Recall initiation date

May 6, 2026

Report date

June 10, 2026

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

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

UPC, lot, and code information

UPC 0399549125016; 1) Cheese Sauce Mix, 25.5 oz.: Product Number: SSP071402 Batch: 045420 through 045424, Lot: 3495, Best By: 12/15/2027 Batch: 046194 through 046198, Lot: 0126, Best By: 01/12/2028 Batch: 047117 through 047120, Lot: 0406, Best By: 02/09/2028 Batch: 047950 through 047953, Lot: 0686, Best By: 03/09/2028 Batch: 049197 and 049200, Lot: 1176, Best By: 04/27/2028 2) Cheese Sauce Mix, 25 lb.: Product Number: SSP071530 Batch: 046520, Lot: 0266, Best By: 01/26/2028 Batch: 048386, Lot: 0826, Best By: 03/23/2028 Batch: 049227, Lot: 1176, Best By: 04/27/2028 3) Creamier Cheese Sauce Mix, 25 lb.: Product Number: SSP071550 Batch: 045307 through 045315 and 045317 through 045324, Lot: 3495, Best By: 12/15/2027 Batch: 046281 through 046297, Lot: 0196, Best By: 01/19/2028 Batch: 047201 through 047218, Lot: 0476, Best By: 02/16/2028 Batch: 048174 through 048192, Lot: 0756, Best By: 03/16/2028 Batch: 048906 through 048911 and 048913 through 048923, Lot: 1036, Best By: 04/13/2026

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 98925 with 3 other product entries in Public Health Trace.

Responsible company: The Coffee Connexion Co., Inc

Other recalls from The Coffee Connexion Co., Inc

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Alabama	1
Arkansas	1
Arizona	1
California	1
Colorado	1
Florida	1
Georgia	1
Illinois	1
Indiana	1
Iowa	1
Kansas	1
Kentucky	1
Louisiana	1
Massachusetts	1
Maryland	1
Maine	1
Michigan	1
Minnesota	1
Missouri	1
Mississippi	1
Montana	1
North Carolina	1
Nebraska	1
New Hampshire	1
New Jersey	1
New Mexico	1
New York	1
Ohio	1
Oklahoma	1
Oregon	1
Pennsylvania	1
Rhode Island	1
South Carolina	1
South Dakota	1
Tennessee	1
Texas	1
Utah	1
Virginia	1
Washington	1
Wisconsin	1
Wyoming	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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