RecallHawk
Class III Recall

Pingo Peanut Butter Cookie Hot Chocolate packaged in single serve pods. Pods are packaged in the following Pingo Varie

TWO RIVERS COFFEE LLC

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

TWO RIVERS COFFEE LLC

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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