KITGREEKPASTA5 1/5# EAST COAST FRESH PC-Greek Pasta Salad Kit recall

Recalled by Sysco Corporation · Houston, TX, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Cucumbers have the potential to be contaminated with Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

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

KITGREEKPASTA5 1/5# EAST COAST FRESH PC-Greek Pasta Salad Kit 1/5lb W/Pasta ALL LOT CODES KITGREEKPASTA5 1/5# EAST COAST FRESH PC-Greek Pasta Salad Kit 1/5lb W/Pasta ALL LOT CODES KITGREEKPASTA51 1/5# EAST COAST FRESH Greek Pasta Salad Kit 1/5lb W/Pasta (RF) ALL LOT CODES

Quantity: 14,338 units (total)

Food: Leafy greens & salads Pasta, rice & grains

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 lot codes

Where it was sold

Connecticut District of Columbia Delaware Florida Georgia Kentucky Massachusetts Maryland Michigan North Carolina New Jersey Ohio Pennsylvania Puerto Rico South Carolina Virginia Vermont West Virginia

FDA's distribution note: DC, DE, FL, GA, MA, MD, MI, NC, NJ, OH, PA, SC, VA, WV, CT, KY, VT and Puerto Rico

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: Sysco Corporation
Initiated by: Voluntary: Firm initiated
Recall initiated: May 21, 2025
In FDA report of: Jun 18, 2025
Terminated: Feb 6, 2026
FDA recall number: H-0024-2025 · event 96923
Official record: FDA enforcement report search