Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 22, 2022 (4 years ago)

Wegmans Organic Baby Kale & Baby Spinach with Sweet Pea Leaves recall

Recalled by Wegmans Food Markets, Inc. · Rochester, NY, United States

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

Why it was recalled

Product(s) may be contaminated with Salmonella.

Pathogen: 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

Wegmans Organic Baby Kale & Baby Spinach with Sweet Pea Leaves; 5 oz

Quantity: 3,360 units microgreens; 1,644 units salad mix

Food: Leafy greens & salads

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.

UPC 77890-52377; Use by date: 12/20/22

Where it was sold

District of Columbia Delaware Massachusetts Maryland North Carolina New Jersey New York Pennsylvania Virginia Washington

FDA's distribution note: MA, NY, PA, NJ, VA, Washington DC, DE, NC, MD

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
Wegmans Food Markets, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 22, 2022
In FDA report of
Feb 1, 2023
Terminated
Mar 28, 2023
FDA recall number
F-0317-2023 · event 91382
Official record
FDA enforcement report search

Also recalled with it (1 more product)

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

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