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Class IITerminated in FDA datasetRecall initiated Feb 25, 2020

Red Pozole Soup Starter, Pozole To The People, packaged in glass jars. Net Wt. 16 fl. oz.,…

Recalling firm: Proxy Foods LLC

Why it was recalled

Missing processing records/production logs. Observations of swollen and/or leaking Red Pozole Starter jars at multiple retail locations.

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: May 29, 2020.

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ProductRed Pozole Soup Starter, Pozole To The People, packaged in glass jars. Net Wt. 16 fl. oz., (473.2 mL). or 24 fl. oz. 16 fl oz UPC 738283379109 24 fl oz UPC 860322002201 The label is read in parts: "***RED POZOLE SOUP STARTER ***NET WT. 24 OZ. ***INGREDIENTS: Water, Hominy, Guajillo, Ancho, Lime Juice, Kosher Salt, Spices*** Refrigerate after opening***Made by Proxy Foods, LLC 7328 SE Foster Road, Portland, OR ***.
Package size16 fl. oz
UPC860322002201

FDA code information

All lot codes

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Full FDA record and distribution details

Original product description

Red Pozole Soup Starter, Pozole To The People, packaged in glass jars. Net Wt. 16 fl. oz., (473.2 mL). or 24 fl. oz. 16 fl oz UPC 738283379109 24 fl oz UPC 860322002201 The label is read in parts: "***RED POZOLE SOUP STARTER ***NET WT. 24 OZ. ***INGREDIENTS: Water, Hominy, Guajillo, Ancho, Lime Juice, Kosher Salt, Spices*** Refrigerate after opening***Made by Proxy Foods, LLC 7328 SE Foster Road, Portland, OR ***.

Extracted codes and context

TypeCode / valueContext
UPC8603220022016 fl. oz., (473.2 mL). or 24 fl. oz. 16 fl oz UPC 738283379109 24 fl oz UPC 860322002201 The label is read in parts: "***RED POZOLE SOUP STARTER ***NET WT. 24 OZ. ***INGREDIENTS: Water, Hominy, Guajillo, A

Original FDA recall reason

Missing processing records/production logs. Observations of swollen and/or leaking Red Pozole Starter jars at multiple retail locations.

Recall details

Recall number
F-0848-2020
Event ID
85097
FDA status
Terminated
Initiated
Feb 25, 2020
Reported
Apr 1, 2020
Classified
Mar 23, 2020
Terminated
May 29, 2020
Quantity
858 units
Location
Portland, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

distributed in Oregon and Washington.

FDA source record · F-0848-2020

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

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