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TWO RIVERS COFFEE LLC Recall: Coffee pods may contain undeclared peanut residue

United States

TerminatedClass III

Company
TWO RIVERS COFFEE LLC
Product
Pingo Peanut Butter Cookie Hot Chocolate packaged in single…
Recall date
January 31, 2023
Terminated
August 16, 2023
Source
FDA

Reason for recall

Coffee pods may contain undeclared peanut residue

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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 810683028150 Approximately 90,000 cups total 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

Distribution

  • Distributed to distributors in WI and WA and distributed nationwide to consumers.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0582-2023
Event ID
91570
Status
Terminated
Classification
Class III
Company
TWO RIVERS COFFEE LLC
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
Quantity
Approximately 90,000 cups total
Reason
Coffee pods may contain undeclared peanut residue
Recall initiation date
January 31, 2023
Report date
March 22, 2023
Classification date
Not published in this source record
Termination date
August 16, 2023
Distribution pattern
Distributed to distributors in WI and WA and distributed nationwide to consumers.
UPC, lot, and code information
UPC 810683028150; 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
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Press Release
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 91570 with 2 other product entries in Public Health Trace.

FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product
Brooklyn Bean Peanut Butter Cup Hot Cocoa packaged in single…
Published
March 22, 2023
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product
Cold Stone Creamery Hot Cocoa Peanut Butter Cup Perfection p…
Published
March 22, 2023
Distribution
Nationwide

View recall →

Responsible company: TWO RIVERS COFFEE LLC

Other recalls from TWO RIVERS COFFEE LLC

FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product
Brooklyn Bean Peanut Butter Cup Hot Cocoa packaged in single…
Published
March 22, 2023
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product
Cold Stone Creamery Hot Cocoa Peanut Butter Cup Perfection p…
Published
March 22, 2023
Distribution
Nationwide

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Wisconsin 1
Washington 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.