Almond Croissant in a clear plastic bag with a white paper label attached to the top of the plastic bag.
Summary
The FDA issued a Class III for Almond Croissant in a clear plastic bag with a white paper label attached to the by SSP America PHX, LLC. Reason: Finished product label stated almond in the product name but did not declare tree nuts or almonds in the ingredients or allergen statement..
Details
Source
Food Recall
External ID
F-1785-2024
Action Date
2024-09-11
Status
Terminated
Category
food
Product Description
Almond Croissant in a clear plastic bag with a white paper label attached to the top of the plastic bag.
Lot/Code Info: Product labels stating Enjoy By: 07/25/24.
Quantity Affected: 27 individual units
Reason for Recall
Finished product label stated almond in the product name but did not declare tree nuts or almonds in the ingredients or allergen statement.
Distribution
AZ
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-19
Company
Phoenix, AZ
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 49 food recalls issued in the same week, part of 204 food-related FDA actions this month.
SSP America PHX, LLC has 6 FDA actions in our database, including 6 recalls.
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 (SSP America PHX, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SSP America PHX, LLC have FDA actions?
SSP America PHX, LLC 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-1785-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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