Check the Batch
Class IITerminated in FDA datasetRecall initiated Oct 17, 2024

GOOD & GATHER 12/9oz GRDL WFL MINI HSTYLE ORG-GDGTR

Recalling firm: Treehouse Foods

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: Aug 11, 2025.

Check your package

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

ProductGOOD & GATHER 12/9oz GRDL WFL MINI HSTYLE ORG-GDGTR UPC 085239343029 H-E-B 12/9oz GRDL WFL MINI HSTYLE ORG-HEBUT UPC 041220708413 365 ORGANIC 12/9oz GRDL WFL MINI HSTYLE ORG - 365OR UPC 099482436995 WEGMANS 12/9oz GRDL WFL MINI HSTYLE ORG - WEGMN UPC 077890481448
Package size9oz
UPC077890481448, 085239343029, 099482436995

FDA code information

All Batch Codes starting with 2C and within shelf-life. Best By Dates: OCT 01 2024 to OCT 11 2025

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

Full FDA record and distribution details

Original product description

GOOD & GATHER 12/9oz GRDL WFL MINI HSTYLE ORG-GDGTR UPC 085239343029 H-E-B 12/9oz GRDL WFL MINI HSTYLE ORG-HEBUT UPC 041220708413 365 ORGANIC 12/9oz GRDL WFL MINI HSTYLE ORG - 365OR UPC 099482436995 WEGMANS 12/9oz GRDL WFL MINI HSTYLE ORG - WEGMN UPC 077890481448

Extracted codes and context

TypeCode / valueContext
UPC077890481448RG - 365OR UPC 099482436995 WEGMANS 12/9oz GRDL WFL MINI HSTYLE ORG - WEGMN UPC 077890481448
UPC085239343029GOOD & GATHER 12/9oz GRDL WFL MINI HSTYLE ORG-GDGTR UPC 085239343029 H-E-B 12/9oz GRDL WFL MINI HSTYLE ORG-HEBUT UPC 041220708413 365 ORGANIC 12/9oz GRDL WFL MINI HSTYLE ORG - 365OR UPC 09
UPC099482436995-HEBUT UPC 041220708413 365 ORGANIC 12/9oz GRDL WFL MINI HSTYLE ORG - 365OR UPC 099482436995 WEGMANS 12/9oz GRDL WFL MINI HSTYLE ORG - WEGMN UPC 077890481448

Original FDA recall reason

potential to be contaminated with Listeria monocytogenes

Recall details

Recall number
F-0206-2025
Event ID
95578
FDA status
Terminated
Initiated
Oct 17, 2024
Reported
Dec 4, 2024
Classified
Nov 27, 2024
Terminated
Aug 11, 2025
Quantity
9,907,389 cases (total)
Location
Oak Brook, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide in USA and Canada

FDA source record · F-0206-2025

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

Follow official FDA and manufacturer guidance.