HANNAFORD 8/12.3oz GRDL WFL MLTGRN-HANNA UPC 041268196319 FOODHOLD 8/12.3oz GRDL WFL MLTGRN-FDHLD UPC 688267081958 H-E-B
Summary
The FDA issued a Class II for HANNAFORD 8/12.3oz GRDL WFL MLTGRN-HANNA UPC 041268196319 FOODHOLD 8/12.3oz GRDL by Treehouse Foods. Reason: potential to be contaminated with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0201-2025
Action Date
2024-12-04
Status
Terminated
Category
food
Product Description
HANNAFORD 8/12.3oz GRDL WFL MLTGRN-HANNA UPC 041268196319 FOODHOLD 8/12.3oz GRDL WFL MLTGRN-FDHLD UPC 688267081958 H-E-B 12/12.3oz GRDL WFL MGRN - HEBUT UPC 041220908233 BEST CHOICE 12/12.3oz GRDL WFL MLTGRN-BSTCH UPC 070038622116 HARRIS TEETER 12/12.3oz GRDL WFL MGRN - HARTE UPC 072036726490 TRADER JOE'S 24/11oz GRDL WFL MGRN - TRDJO UPC 000000199681
Lot/Code Info: All Batch Codes starting with 2C and within shelf-life. Best By Dates: OCT 01 2024 to OCT 11 2025
Quantity Affected: 9,907,389 cases (total)
Reason for Recall
potential to be contaminated with Listeria monocytogenes
Distribution
Nationwide in USA and Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-17
Company
Oak Brook, IL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 82 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Treehouse Foods has 69 FDA actions in our database, including 69 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Treehouse Foods) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Treehouse Foods have FDA actions?
Treehouse Foods has 69 FDA actions in our database, including 69 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0201-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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