RecallHawk
Class I Recall

Geissler's Supermarket Shrimp Tempura and Lobster Roll 12 oz.

Geissler's Supermarket

Summary

The FDA issued a Class I for Geissler's Supermarket Shrimp Tempura and Lobster Roll 12 oz. by Geissler's Supermarket. Reason: undeclared allergens (wheat).

Details

Source

Food Recall

External ID

F-1256-2024

Action Date

2024-05-29

Status

Terminated

Category

food

Product Description

Geissler's Supermarket Shrimp Tempura and Lobster Roll 12 oz.

Lot/Code Info: Sell by date of 3/27/2024, and 3/28/2024 UPC:23410400000 12 oz. UPC Codes: 234104011994

Quantity Affected: 193 units total

Reason for Recall

undeclared allergens (wheat)

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 I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

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 I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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-1256-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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