RecallHawk
Class III Recall

Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich 3 pk units - 8.75 oz (2.9 oz./unit) UPC: 8 5000988328 5

Perfect Day Inc

Summary

The FDA issued a Class III for Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich 3 pk units - 8.75 by Perfect Day Inc. Reason: Presence of coliform found in 3rd party lab samples.

Details

Source

Food Recall

External ID

F-0179-2023

Action Date

2022-12-07

Status

Terminated

Category

food

Product Description

Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich 3 pk units - 8.75 oz (2.9 oz./unit) UPC: 8 5000988328 5 Distributed by Coolhaus 8688 Washington Blvd. Culver City, CA 90232

Lot/Code Info: Best By Date: 3/19/2024

Quantity Affected: 284 cases

Reason for Recall

Presence of coliform found in 3rd party lab samples

Distribution

Product was shipped only to consignee, KeHE Distributors, with locations in TX, MD, CO, and CA

Type: Voluntary: Firm initiated

Recall Initiated: 2022-11-02

Company

Perfect Day Inc

Berkeley, CA

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 16 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Perfect Day Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Perfect Day Inc have FDA actions?

This is the only FDA action we have on record for Perfect Day Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0179-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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