Food Recall Check
Class II · Moderate risk Terminated Initiated Jul 6, 2023 (3 years ago)

SPRING VALLEY brand POTATO BLINTZES recall

Recalled by Milmar Food Corp · Goshen, NY, United States

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

Why it was recalled

Product contains 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

SPRING VALLEY brand POTATO BLINTZES; NET WT. 13 OZ (369g); KEEP FROZEN; READY TO COOK; INGREDIENTS: WHEAT FLOUR (WHET FLOUR, NIACIN, REDUCED IRON, THIAMIN MONONITRATE, RIBOFLAVEN, ENZYME, FOLIC ACID), WATER, POTATOES, EGG, ONIONS, CANOLA OIL, EGG WHITES, DEXTROSE, CORN STARCH, SALT, SUGAR, GARLIC, ONION POWDER, SOY LECITHIN, SPICES.; ALLERGEN INFORMATION: CONTAINS EGG, SOY, WHEAT; PREPARED BY: MILMAR FOOD GROUP, LLC GOSHEN, NY 10924

Quantity: 100 cases

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# 1513MMR7831RE UPC: 8 13801 00321 3

Where it was sold

Florida Maryland New Jersey New York

FDA's distribution note: NY, NJ, MD, FL

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
Milmar Food Corp
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 6, 2023
In FDA report of
Aug 2, 2023
Terminated
Aug 21, 2023
FDA recall number
F-1292-2023 · event 92661
Official record
FDA enforcement report search