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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Packaged & Processed

Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich Recalled for Coliform

Agency Publication Date: November 28, 2022
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Summary

Perfect Day Inc. is voluntarily recalling approximately 284 cases of Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich (3-pack units, 8.75 oz). The recall was initiated after third-party laboratory samples detected the presence of coliform. No incidents or illnesses have been reported to date in connection with this product.

Risk

The presence of coliform bacteria indicates that the food may have been produced under unsanitary conditions, though it is used primarily as an indicator of process failure rather than a specific pathogen.

What You Should Do

  1. The recalled products are 3-pack units (8.75 oz) of Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich with UPC 850009883285 and a Best By Date of 3/19/2024.
  2. Return the product to the place of purchase for a refund, throw it away, or contact Perfect Day Inc for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for more information regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich (8.75 oz)
Variants: 3 pk units, 2.9 oz./unit
UPC Codes:
850009883285
Date Ranges: Best By Date: 3/19/2024

Recall #: F-0179-2023; Distributed by Coolhaus, 8688 Washington Blvd., Culver City, CA 90232

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91118
Status: Resolved
Manufacturer: Perfect Day Inc
Sold By: KeHE Distributors
Manufactured In: United States
Units Affected: 284 cases
Distributed To: Texas, Maryland, Colorado, California

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.