Check the Batch
Class IITerminated in FDA datasetFeb 17, 2023

Kirkland Signature Colombian Cold Brew Coffee ready-to-drink, 12 fl oz in aluminum can, 12 cans per case

Recalling firm: Berner Foods Inc.

Why it was recalled

Foreign material, metal

Check your package

Compare the exact product and package details with the label you have.

ProductKirkland Signature Colombian Cold Brew Coffee ready-to-drink, 12 fl oz in aluminum can, 12 cans per case

FDA code information

Lot#231019 Best If Used By: 10 19 23; Lot#231020 Best If Used By: 10 20 23; Lot#231021 Best If Used By: 10 21 23; Lot#231022 Best If Used By: 10 22 23; Lot#231023 Best If Used By: 10 23 23; Lot#231024 Best If Used By; 10 24 23; Lot#231025 Best If Used By: 10 25 23; Lot#231026 Best If Used By: 10 26 23; Lot#231027 Best If Used By: 10 27 23

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Kirkland Signature Colombian Cold Brew Coffee ready-to-drink, 12 fl oz in aluminum can, 12 cans per case

Extracted codes and context

TypeCode / valueContext
lot231019Lot#231019 Best If Used By: 10 19 23; Lot#231020 Best If Used By: 10 20 23; Lot#231021 Best If Used By: 10 21 23; Lot#231022 Best
lot231020Lot#231019 Best If Used By: 10 19 23; Lot#231020 Best If Used By: 10 20 23; Lot#231021 Best If Used By: 10 21 23; Lot#231022 Best If Used By: 10 22 23; Lot#231023 Best
lot231021Lot#231019 Best If Used By: 10 19 23; Lot#231020 Best If Used By: 10 20 23; Lot#231021 Best If Used By: 10 21 23; Lot#231022 Best If Used By: 10 22 23; Lot#231023 Best If Used By: 10 23 23; Lot#231024 Best
lot231022Lot#231020 Best If Used By: 10 20 23; Lot#231021 Best If Used By: 10 21 23; Lot#231022 Best If Used By: 10 22 23; Lot#231023 Best If Used By: 10 23 23; Lot#231024 Best If Used By; 10 24 23; Lot#231025 Best
lot231023Lot#231021 Best If Used By: 10 21 23; Lot#231022 Best If Used By: 10 22 23; Lot#231023 Best If Used By: 10 23 23; Lot#231024 Best If Used By; 10 24 23; Lot#231025 Best If Used By: 10 25 23; Lot#231026 Best
lot231024Lot#231022 Best If Used By: 10 22 23; Lot#231023 Best If Used By: 10 23 23; Lot#231024 Best If Used By; 10 24 23; Lot#231025 Best If Used By: 10 25 23; Lot#231026 Best If Used By: 10 26 23; Lot#231027 Best
lot231025Lot#231023 Best If Used By: 10 23 23; Lot#231024 Best If Used By; 10 24 23; Lot#231025 Best If Used By: 10 25 23; Lot#231026 Best If Used By: 10 26 23; Lot#231027 Best If Used By: 10 27 23
lot231026Lot#231024 Best If Used By; 10 24 23; Lot#231025 Best If Used By: 10 25 23; Lot#231026 Best If Used By: 10 26 23; Lot#231027 Best If Used By: 10 27 23
lot231027Lot#231025 Best If Used By: 10 25 23; Lot#231026 Best If Used By: 10 26 23; Lot#231027 Best If Used By: 10 27 23

Recall details

Recall number
F-0648-2023
Event ID
91742
FDA status
Terminated
Initiated
Feb 17, 2023
Reported
Mar 29, 2023
Classified
Mar 21, 2023
Terminated
Feb 23, 2024
Quantity
231,071 cases (2,772,852 cans)
Location
Dakota, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

GA, NJ, CA, MD, MI, IL, WA, AZ, UT, FL, CO, TX, MN

FDA source record · F-0648-2023

Data updated September 16, 2026. View official FDA data ↗

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