Pingo Peanut Butter Cookie Hot Chocolate packaged in single serve pods. Pods are packaged in the following Pingo Varie
Summary
The FDA issued a Class III for Pingo Peanut Butter Cookie Hot Chocolate packaged in single serve pods. Pods a by TWO RIVERS COFFEE LLC. Reason: Coffee pods may contain undeclared peanut residue.
Details
Source
Food Recall
External ID
F-0582-2023
Action Date
2023-03-22
Status
Terminated
Category
food
Product Description
Pingo Peanut Butter Cookie Hot Chocolate packaged in single serve pods. Pods are packaged in the following Pingo Variety Pack boxes: Pingo Hot Chocolate Pods Variety Pack, 40 Count UPC: 810683028150 Pingo Hot Chocolate Pods Variety Pack, 100 Count UPC: 810683029805 Pingo Hot Chocolate Pods Peanut Butter Cookie, 100 Count UPC: 810683028754 Pingo Hot Chocolate Pods Peanut Butter Cookie, 40 Count UPC: 810683028037
Lot/Code Info: AGG-PB021102, AGG-PB021701 , AGG-1121079, AGG-1121081, AGG-0222067, AGG-PB021001, AGG-PB021702 , AGG-PB021703, AGG-0322032, AGG-0422015 AGG-1122045, AGG-0322033, AGG-0422013
Quantity Affected: Approximately 90,000 cups total
Reason for Recall
Coffee pods may contain undeclared peanut residue
Distribution
Distributed to distributors in WI and WA and distributed nationwide to consumers.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-01-31
Company
South Plainfield, 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 488 food recalls issued in the same week, part of 204 food-related FDA actions this month.
TWO RIVERS COFFEE LLC has 3 FDA actions in our database, including 3 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 (TWO RIVERS COFFEE LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does TWO RIVERS COFFEE LLC have FDA actions?
TWO RIVERS COFFEE LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0582-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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