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Food FDA Class I Ongoing Pathogen contamination

Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0039954921963

The Coffee Connexion Co., Inc Published Jun 10, 2026

Risk level

Class I

Dangerous or defective — could cause serious health problems or death.

Severity score 100/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact The Coffee Connexion Co., Inc or your place of purchase with questions, and see the source record below for full details.
Reason for recall

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

Hazards

Salmonella · primary

Affected products (1)

Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0039954921963

913 cases

Lot codes: 0126, 0476, 0686, 1106
Code info: Product Number: SSP980713 Batch: 046188 through 046193, Lot: 0126, Best By: 01/12/2028 Batch: 047290 through 047296, Lot: 0476, Best By: 02/16/2028 Batch: 048029 through 048034, Lot: 0686, Best By: 03/09/2028 Batch: 049089 through 049094, Lot: 1106, Best By: 04/20/2028

Affected areas

AlabamaArizonaArkansasCaliforniaColoradoFloridaGeorgiaIllinoisIndianaIowaKansasKentuckyLouisianaMaineMarylandMassachusettsMichiganMinnesotaMississippiMissouriMontanaNebraskaNew HampshireNew JerseyNew MexicoNew YorkNorth CarolinaOhioOklahomaOregonPennsylvaniaRhode IslandSouth CarolinaSouth DakotaTennesseeTexasUtahVirginiaWashingtonWisconsinWyoming

Timeline

  1. Initiated
    May 6, 2026
  2. Published
    Jun 10, 2026
Recall number
H-0909-2026
Agency
U.S. Food and Drug Administration
Country
US

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.