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Class II: temporary or reversible health riskTerminated

Popsalot Moroccan Mystique 3 Recall

Popsalot Moroccan Mystique 3

POPSALOT, LLC · Paramount, CA

Risk level
Class II
Reported by FDA
Sep 28, 2016
Recall ID
F-2285-2016
Check your lot numberHow we source this data

Summary

Popsalot recalled Popsalot Moroccan Mystique 3 starting May 5, 2016. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2285-2016 on Sep 28, 2016. Reason: Gluten levels above regulatory threshold. Status: Terminated.

Why it was recalled

Gluten levels above regulatory threshold.

Product description

Popsalot Moroccan Mystique 3.5 oz

Lot numbers, UPCs & expiration codes

2250,6020

Where it was sold

U.S. distribution to the following; CA No foreign distribution.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-2285-2016
Classification
Class II
Status
Terminated
Recall initiated
May 5, 2016
FDA report date
Sep 28, 2016
Quantity
165 cases
Recall type
Voluntary: Firm initiated
Recalling firm
POPSALOT, LLC

Original FDA data

Every field from FDA enforcement report F-2285-2016, exactly as published.

Show all FDA fields
City
Paramount
State
CA
Status
Terminated
Country
United States
Event ID
74132
Address
7723 Somerset Blvd
Code information
2250,6020
Postal code
90723-4104
Report date
Sep 28, 2016
Product type
Food
Recall number
F-2285-2016
Classification
Class II
Recalling firm
POPSALOT, LLC
Product quantity
165 cases
Termination date
Oct 27, 2016
Reason for recall
Gluten levels above regulatory threshold.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Popsalot Moroccan Mystique 3.5 oz
Distribution pattern
U.S. distribution to the following; CA No foreign distribution.
Recall initiation date
May 5, 2016
Initial firm notification
E-Mail
Center classification date
Sep 16, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2285-2016, published Sep 28, 2016. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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