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US alfredo sauce recalled for potential salmonella contamination
๐Ÿ‡บ๐Ÿ‡ธ United States /Health & Science

US alfredo sauce recalled for potential salmonella contamination

From PBS NewsHour · () English

Translated from English, summarized and contextualized by DistantNews.

At a glance

News From a news agency New plan
  • A recall has been issued for alfredo sauce distributed across the U.S. due to potential salmonella contamination.
  • The supplier voluntarily recalled the sauce because it contained a dry milk powder ingredient possibly contaminated with salmonella.
  • The FDA designated the recall as its highest risk category, warning of potential serious adverse health effects.

Federal health officials have initiated a recall for alfredo sauce supplied to numerous U.S. states, citing concerns over potential salmonella contamination. The supplier, The Coffee Connexion Co. Inc. based in Lebanon, Tennessee, voluntarily initiated the recall.

The company cited a dry milk powder ingredient as the source of the potential contamination. According to a U.S. Food and Drug Administration enforcement report, 913 cases of the sauce were recalled. Each case contained 12 sealed bags, with each bag weighing over 3 pounds (1.36 kilograms).

The sauce was voluntarily recalled by the supplier because it contained a dry milk powder ingredient that was possibly contaminated with salmonella, according to a U.S. Food and Drug Administration enforcement report.

โ€” U.S. Food and Drug AdministrationExplaining the reason for the voluntary recall of the alfredo sauce.

The FDA has classified the recall under its highest risk category. This designation indicates a reasonable probability that the product could cause serious adverse health issues or even death. Symptoms of salmonella poisoning typically appear within 12 to 72 hours after consumption and include diarrhea, fever, and abdominal cramps, usually lasting four to seven days.

Individuals at higher risk for severe infections include children, people over 65, and those with weakened immune systems. The FDA did not immediately respond to requests for further information on the matter.

The recall, which was initiated last month, was designated earlier this month by the FDA as its highest risk category: one in which there was a reasonable probability that the product could cause serious adverse health issues or death.

โ€” U.S. Food and Drug AdministrationDetailing the severity and risk level assigned to the product recall.
DistantNews Editorial

Originally published by PBS NewsHour in English. Translated, summarized, and contextualized by our editorial team with added local perspective. Read our editorial standards.