Food Recall Check
Class II · Moderate risk Terminated Initiated May 6, 2022 (4 years ago)

Spinach-Feta Pierogi Grandma s Cuisine Spinach-Feta Pierogi recall

Recalled by Dymski Pierogi LLC · E Stroudsburg, PA, United States

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

Why it was recalled

Undeclared milk

Undeclared allergen: Milk

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Spinach-Feta Pierogi Grandma s Cuisine Spinach-Feta Pierogi UPC: 8 67355 00037 2 14oz (397g) / 1 dozen Golden Eagle Spinach & Feta Pierogis 16 oz (454g) Bernat s Spinach and Feta Cheese 16oz (450g)

Quantity: 865 units

Food: Cheese 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.

all lots

Where it was sold

Massachusetts New Jersey Pennsylvania

FDA's distribution note: Distributed to retail stores, restaurants, and distribution centers in NJ, MA, and PA.

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. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. 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
Dymski Pierogi LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
May 6, 2022
In FDA report of
Jun 8, 2022
Terminated
Oct 25, 2022
FDA recall number
F-1099-2022 · event 90144
Official record
FDA enforcement report search

Also recalled with it (8 more products)

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