Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 28, 2024 (3 years ago)

Geissler's Supermarket Philadelphia Avo or Cucumber Classic Roll recall

Recalled by Geissler's Supermarket · East Windsor, CT, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

undeclared allergens (milk)

Undeclared allergen: Milk

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Geissler's Supermarket Philadelphia Avo or Cucumber Classic Roll (sushi roll) Ingredients read in part: "***INGREDIENTS: SMOKED SALMON, CREAM CHEESE, AVOCADO, CUCUMBER, RICE. NORI. WHITE STEAMEDRICE. VINEGAR. SUGAR. SALT. LEMON. MIRIN.WASABI. GINGER. WATER, SOYSAUCE (WHEAT, SOYBEANS, ALCOHOL)***MADE IN A FACILITY THAT PROCESSES SHELLFISH,SOY, PEANUTS, TREE NUTS, EGGS, DAIRY & WHEAT***"

Quantity: 193 units total

Food: Cucumbers Salads, sandwiches & prepared foods

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Sell by date of 3/27/2024, and 3/28/2024 UPC:23404400000

Where it was sold

Connecticut Massachusetts

FDA's distribution note: CT & MA

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Geissler's Supermarket
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 28, 2024
In FDA report of
May 29, 2024
Terminated
Jun 14, 2024
FDA recall number
F-1251-2024 · event 94311
Official record
FDA enforcement report search

Also recalled with it (5 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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