Wegmans 12/ recall

Recalled by Treehouse Foods · Oak Brook, IL, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

potential to be contaminated with Listeria monocytogenes

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

WEGMANS 12/7.4oz GRDL WFL FLAX ORG - WEGMN UPC 077890481424 H-E-B 12/8.25oz GRDL WFL FLAX ORG-HEBUT UPC 041220708338 WEGMANS 12/8.25OZ 6CT GRDL WFL FLAX ORG-WEGMN UPC 077890577059 NATURES PATH ORGANIC 12/7.4oz GRDL WFL FLAX ORG - NPTHO UPC 058449590569 NATURES PATH ORGANIC 12/210g GRDL WFL FLAX ORG-NPOCN UPC 058449590552 CENTRAL MARKET 12/8.25oz GRDL WFL FLAX ORG - CTMKT UPC 041220198658

Quantity: 9,907,389 cases (total)

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Nationwide.

FDA's distribution note: Nationwide in USA and Canada

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Treehouse Foods
Initiated by: Voluntary: Firm initiated
Recall initiated: Oct 17, 2024
In FDA report of: Dec 4, 2024
Terminated: Aug 11, 2025
FDA recall number: F-0193-2025 · event 95578
Official record: FDA enforcement report search

Also recalled with it (64 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Listeria Oct 17, 2024