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Class ITerminated in FDA datasetRecall initiated Nov 14, 2012

Berres Brothers Coffee Roasters Lunch with Elvis regular ground coffee packaged in the…

Recalling firm: Berres Brothers, Inc.

Why it was recalled

Berres Brothers Coffee Roasters is recalling 3 flavors of regular and decaffeinated, ground and whole bean coffees because they contain undeclared walnut. Chocolate & Peanut…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 31, 2013.

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

ProductBerres Brothers Coffee Roasters Lunch with Elvis regular ground coffee packaged in the following sizes: 1.5 oz. (42.5g) with UPC 746774-000425, and 12 oz. (340g) bags with no UPC.
Package size1.5 oz
UPC746774000425

FDA code information

Julian date codes 12091 - 12319 (April 1, 2012 thru November 15, 2012)

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Full FDA record and distribution details

Original product description

Berres Brothers Coffee Roasters Lunch with Elvis regular ground coffee packaged in the following sizes: 1.5 oz. (42.5g) with UPC 746774-000425, and 12 oz. (340g) bags with no UPC.

Extracted codes and context

TypeCode / valueContext
UPC746774000425egular ground coffee packaged in the following sizes: 1.5 oz. (42.5g) with UPC 746774-000425, and 12 oz. (340g) bags with no UPC.

Original FDA recall reason

Berres Brothers Coffee Roasters is recalling 3 flavors of regular and decaffeinated, ground and whole bean coffees because they contain undeclared walnut. Chocolate & Peanut Butter, Monkey Mocha, and Lunch with Elvis

Recall details

Recall number
F-0816-2013
Event ID
63696
FDA status
Terminated
Initiated
Nov 14, 2012
Reported
Dec 19, 2012
Classified
Dec 12, 2012
Terminated
Jan 31, 2013
Quantity
9998 packages
Location
Watertown, WI, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

AL, AK, AZ, AR, CA, CO, CT, FL, GA, IL, IN, IA, KS, KY, MD, MI, MN, MS,MO, MT, NE, NV, NH, NJ, NY, NC, ND, OH, OK, OR, PA, SC,SD, TN, TX, VA, WA, AW, WI, WY. OUS: GU, AE, CA

FDA source record · F-0816-2013

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

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