Weis Original Potato Salad
Reason Undeclared milk.
Sliced (1/4") green onions recall
Recalled by Garden Fresh Foods, Inc. · Woodinville, WA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Possible positive Listeria monocytogenes. Firm tested one lot of sliced green onions in-house and found 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
Sliced (1/4") green onions, refrigerated, packaged in plastic bag. Each case consist 5/6lbs. bag (net wt. 30lbs.). Garden Fresh Foods Inc. Woodinville, WA. Product is distributed in bulk package and is not sold directly to consumers.
Quantity: 540 lbs. total
Food: Onions
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.
Mfg code: 09/15/25 Lot Code: 09/15/25 Use Before: 09/22/25 Internal traceability code: Lot #OG25251MUXX
Where it was sold
Washington
FDA's distribution note: Distributed in WA only
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
- Garden Fresh Foods, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 18, 2025
- In FDA report of
- Oct 22, 2025
- Terminated
- Nov 25, 2025
- FDA recall number
- H-0035-2026 · event 97740
- Official record
- FDA enforcement report search
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