RecallHawk
Class I Recall

Weis Quality Brownie Moose Tracks Ice Cream (48oz)UPC of 041497-01194 Packaged in a scround container. 6 units per case.

Weis Markets, Inc., Ice Cream Division

Summary

The FDA issued a Class I for Weis Quality Brownie Moose Tracks Ice Cream (48oz)UPC of 041497-01194 Packaged i by Weis Markets, Inc., Ice Cream Division. Reason: Undeclared egg.

Details

Source

Food Recall

External ID

F-1617-2023

Action Date

2023-10-04

Status

Terminated

Category

food

Product Description

Weis Quality Brownie Moose Tracks Ice Cream (48oz)UPC of 041497-01194 Packaged in a scround container. 6 units per case.

Lot/Code Info: All lots

Quantity Affected: total = 1814 containers & 2045 cases

Reason for Recall

Undeclared egg

Distribution

Retail locations in the following states: DE, MD, NJ, NY, PA, VA, WV

Type: Voluntary: Firm initiated

Recall Initiated: 2023-08-30

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 185 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Weis Markets, Inc., Ice Cream Division 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 (Weis Markets, Inc., Ice Cream Division) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Weis Markets, Inc., Ice Cream Division have FDA actions?

Weis Markets, Inc., Ice Cream Division 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-1617-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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