Class ITerminated in FDA datasetRecall initiated Oct 1, 2020

Seasonal Blend 10oz

Recalling firm: Country Fresh Inc.

Why it was recalled

Potential to be contaminated with Listeria monocytogenes

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: Dec 16, 2020.

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ProductSeasonal Blend 10oz UPC 68113118048; Seasonal Blend 16oz UPC 681131180498; Seasonal Blend 32oz UPC 681131180504 all packaged in clear plastic containers
Package size10oz
UPC681131180498, 681131180504

FDA code information

Best Before 10/02-11/2020; Lot# URE0203 Lot# URS0203 Lot# URE0203 Lot# URS0203 Lot# URS0203 Lot# URS0203

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Full FDA record and distribution details

Original product description

Seasonal Blend 10oz UPC 68113118048; Seasonal Blend 16oz UPC 681131180498; Seasonal Blend 32oz UPC 681131180504 all packaged in clear plastic containers

Extracted codes and context

TypeCode / valueContext
UPC681131180498Seasonal Blend 10oz UPC 68113118048; Seasonal Blend 16oz UPC 681131180498; Seasonal Blend 32oz UPC 681131180504 all packaged in clear plastic containers
UPC681131180504 UPC 68113118048; Seasonal Blend 16oz UPC 681131180498; Seasonal Blend 32oz UPC 681131180504 all packaged in clear plastic containers
lotURE0203Best Before 10/02-11/2020; Lot# URE0203 Lot# URS0203 Lot# URE0203 Lot# URS0203 Lot# URS0203 Lot# URS0203
lotURS0203Best Before 10/02-11/2020; Lot# URE0203 Lot# URS0203 Lot# URE0203 Lot# URS0203 Lot# URS0203 Lot# URS0203
lotURS0203e 10/02-11/2020; Lot# URE0203 Lot# URS0203 Lot# URE0203 Lot# URS0203 Lot# URS0203 Lot# URS0203
lotURS02030; Lot# URE0203 Lot# URS0203 Lot# URE0203 Lot# URS0203 Lot# URS0203 Lot# URS0203

Original FDA recall reason

Potential to be contaminated with Listeria monocytogenes

Recall details

Recall number
F-0085-2021
Event ID
86538
FDA status
Terminated
Initiated
Oct 1, 2020
Reported
Oct 21, 2020
Classified
Nov 5, 2020
Terminated
Dec 16, 2020
Quantity
36983 cases (total)
Location
Grand Prairie, TX, 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

AR, IL, IN, KS, KY, LA, MO, OK, and TX.

FDA source record · F-0085-2021

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

Follow official FDA and manufacturer guidance.