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Jelly Recall Update as FDA Sets Risk Level

Jelly Recall Update as FDA Sets Risk Level

Summary

The U.S. FDA has classified a recall of Prickly Pear Jelly by The Maros Group, LLC, as a Class II risk due to an undeclared milk allergen. The recalled jelly was distributed only in Arizona and affects certain lot codes with specific sell-by dates.

Key Facts

  • The recall involves Prickly Pear Jelly bottles with an undeclared milk allergen.
  • The affected product consists of 24 bottles in total, each holding 9 ounces of jelly.
  • The recall applies to specific lot codes with sell-by dates in April, May, and June 2026.
  • The recall is classified as a Class II by the FDA, which means it may cause temporary or reversible health effects.
  • Only Arizona received the distributed product, and no public press release was initiated.
  • Milk is one of the nine major allergens identified by the FDA and can cause severe reactions in allergic individuals.
  • Customers with milk allergies should avoid consuming this recalled jelly.
  • Consumers can contact the FDA for further instructions as no refund details are provided.
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