RecallHawk
Class II Recall

WOW! Factor Desserts Berry Burst Slab Cake. Weight 2x8.15lbs UPC:10778463085373 Packaged in paper cartons.

Wow Factor Desserts

Summary

The FDA issued a Class II for WOW! Factor Desserts Berry Burst Slab Cake. Weight 2x8.15lbs UPC:10778463085373 by Wow Factor Desserts. Reason: Possible norovirus contamination.

Details

Source

Food Recall

External ID

F-1344-2023

Action Date

2023-08-09

Status

Terminated

Category

food

Product Description

WOW! Factor Desserts Berry Burst Slab Cake. Weight 2x8.15lbs UPC:10778463085373 Packaged in paper cartons.

Lot/Code Info: 3101, 3114, 3121, and 3124

Quantity Affected: 333 Cases

Reason for Recall

Possible norovirus contamination

Distribution

Distributed to distributors in CO, PA, OH and MI.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-06-12

Company

Wow Factor Desserts

Sherwood Park, N/A

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

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 (Wow Factor Desserts) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Wow Factor Desserts have FDA actions?

This is the only FDA action we have on record for Wow Factor Desserts in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1344-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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