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Class IITerminated in FDA datasetRecall initiated Jan 9, 2015

Oregon Microbrew BBQ Sauce, Paradigm and Fess Parker brand, net wt. 12 fl. oz. (343 mL). The…

Recalling firm: Paradigm Foodworks, Inc

Why it was recalled

Microbrew BBQ Sauce containing mild chili powder, is recalled due to potential for contamination with peanut protein.

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: Aug 25, 2015.

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ProductOregon Microbrew BBQ Sauce, Paradigm and Fess Parker brand, net wt. 12 fl. oz. (343 mL). The Paradigm has the UPC 0-37644-30520-8. The Fess Parker brand does not have UPC. The advisory statement on label is read "Made in a facility that handles peanuts, tree nuts, eggs, milk, wheat, soybeans, and fish".
Package size12 fl. oz
UPC037644305208

FDA code information

Best By Date: 12/4/2016 Lot code: 33814-10

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Full FDA record and distribution details

Original product description

Oregon Microbrew BBQ Sauce, Paradigm and Fess Parker brand, net wt. 12 fl. oz. (343 mL). The Paradigm has the UPC 0-37644-30520-8. The Fess Parker brand does not have UPC. The advisory statement on label is read "Made in a facility that handles peanuts, tree nuts, eggs, milk, wheat, soybeans, and fish".

Extracted codes and context

TypeCode / valueContext
UPC037644305208and Fess Parker brand, net wt. 12 fl. oz. (343 mL). The Paradigm has the UPC 0-37644-30520-8. The Fess Parker brand does not have UPC. The advisory statement on label is read "Made in a facility that handles

Original FDA recall reason

Microbrew BBQ Sauce containing mild chili powder, is recalled due to potential for contamination with peanut protein.

Recall details

Recall number
F-2840-2015
Event ID
70300
FDA status
Terminated
Initiated
Jan 9, 2015
Reported
Jul 15, 2015
Classified
Jul 8, 2015
Terminated
Aug 25, 2015
Quantity
47 cases (6/12 fl. oz. bottles per case)
Location
Lake Oswego, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

distributed directly to Idaho, California, Oregon and Washington and in Ontario, Canada.

FDA source record · F-2840-2015

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

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