Kale Net Wt
Reason The firm was notified by one of their customers that during a random testing by ODA the product test positive for Listeria monocytogenes.
Baker Farms CURLY MUSTARD recall
Recalled by Terry and Joe Baker Farms, LLC dba Baker Farms · Norman Park, GA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The firm was notified by the Texas Department of Agriculture that the product test positive for Listeria monocytogenes.
Pathogen: Listeria
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
Baker Farms CURLY MUSTARD 16 oz NET WT 16 oz UPC 8 13098 02018 4 Baker Farms 3667 Ellenton-Norman Park Road Norman Park, GA 31771
Quantity: 449cs/8/16oz bags
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.
Lot code: bak144-6806 BEST BY 11-21-2024
Where it was sold
Alabama Arkansas Florida Georgia Kentucky Louisiana Mississippi Tennessee Texas
FDA's distribution note: Product was shipped to distribution centers in the following states: AL, AR, FL, GA, KY, LA, MS, TN & TX.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
- Terry and Joe Baker Farms, LLC dba Baker Farms
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 29, 2024
- In FDA report of
- Dec 25, 2024
- Terminated
- Jan 9, 2026
- FDA recall number
- F-0302-2025 · event 95877
- Official record
- FDA enforcement report search