RecallHawk
Class II Recall

Geissler's Supermarket Philadelphia Avo or Cucumber Classic Roll (sushi roll) Ingredients read in part: "***INGREDIENTS

Geissler's Supermarket

Summary

The FDA issued a Class II for Geissler's Supermarket Philadelphia Avo or Cucumber Classic Roll (sushi roll) I by Geissler's Supermarket. Reason: undeclared allergens (milk).

Details

Source

Food Recall

External ID

F-1251-2024

Action Date

2024-05-29

Status

Terminated

Category

food

Product Description

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***"

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

Quantity Affected: 193 units total

Reason for Recall

undeclared allergens (milk)

Distribution

CT & MA

Type: Voluntary: Firm initiated

Recall Initiated: 2024-03-28

Company

Geissler's Supermarket

East Windsor, CT

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 27 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Geissler's Supermarket has 6 FDA actions in our database, including 6 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Geissler's Supermarket) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Geissler's Supermarket have FDA actions?

Geissler's Supermarket has 6 FDA actions in our database, including 6 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1251-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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