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

WEGMANS 12/16.5oz GRDL PNCK BB-WEGMN

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.

ProductWEGMANS 12/16.5oz GRDL PNCK BB-WEGMN UPC 077890481387 YELLOH 12/16.5oz GRDL PNCK BLBRY-YLLOH UPC 810038684680 GIANT EAGLE 12/16.5oz GRDL PNCK BLBRY-GT/EG UPC 030034011673
Package size16.5oz
UPC030034011673, 077890481387, 810038684680

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

WEGMANS 12/16.5oz GRDL PNCK BB-WEGMN UPC 077890481387 YELLOH 12/16.5oz GRDL PNCK BLBRY-YLLOH UPC 810038684680 GIANT EAGLE 12/16.5oz GRDL PNCK BLBRY-GT/EG UPC 030034011673

Extracted codes and context

TypeCode / valueContext
UPC030034011673CK BLBRY-YLLOH UPC 810038684680 GIANT EAGLE 12/16.5oz GRDL PNCK BLBRY-GT/EG UPC 030034011673
UPC077890481387WEGMANS 12/16.5oz GRDL PNCK BB-WEGMN UPC 077890481387 YELLOH 12/16.5oz GRDL PNCK BLBRY-YLLOH UPC 810038684680 GIANT EAGLE 12/16.5oz GRDL PNCK BLBRY-GT/EG UPC 030034011673
UPC810038684680 GRDL PNCK BB-WEGMN UPC 077890481387 YELLOH 12/16.5oz GRDL PNCK BLBRY-YLLOH UPC 810038684680 GIANT EAGLE 12/16.5oz GRDL PNCK BLBRY-GT/EG UPC 030034011673

Original FDA recall reason

potential to be contaminated with Listeria monocytogenes

Recall details

Recall number
F-0153-2025
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-0153-2025

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

Follow official FDA and manufacturer guidance.