Cocoa de Aroma, 24 ct single serve coffee pods assorted (12.7 oz carton containing Peanut Butter flavor 0.52 oz. single
Summary
The FDA issued a Class III for Cocoa de Aroma, 24 ct single serve coffee pods assorted (12.7 oz carton containi by Corim International Coffee Inc.. Reason: Corim Industries, 1112 Industrial Parkway, Brick, NJ 08724 is initiating a recall of Agglomerated Peanut Butter Hot Chocolate, Peanut Butter Cappuccin.
Details
Source
Food Recall
External ID
F-0387-2023
Action Date
2023-03-08
Status
Terminated
Category
food
Product Description
Cocoa de Aroma, 24 ct single serve coffee pods assorted (12.7 oz carton containing Peanut Butter flavor 0.52 oz. single serve coffee pods)
Lot/Code Info: All lots with Best By dates between January 11, 2023 and January 11, 2025
Quantity Affected: (Smart Sips Packets- 4,800)(Smart Sips Cups- 11,521)(Direct (Fundraiser)-576 cups)(Colonial Coffee- 1,536 cups)(CM Coffee- 21,252 Cups) (Intelligent
Reason for Recall
Corim Industries, 1112 Industrial Parkway, Brick, NJ 08724 is initiating a recall of Agglomerated Peanut Butter Hot Chocolate, Peanut Butter Cappuccino, 500lb sacks; single serve cups (15g), single serve packets (28g) because of undeclared peanut allergen.
Distribution
The product was distributed to the following states: NJ, CA, NY, IL,
Type: Voluntary: Firm initiated
Recall Initiated: 2023-01-13
Company
Brick, NJ
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 45 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Corim International Coffee Inc. has 4 FDA actions in our database, including 4 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 (Corim International Coffee Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Corim International Coffee Inc. have FDA actions?
Corim International Coffee Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0387-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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