Food Recall Check
Class II · Moderate risk Terminated Initiated May 13, 2022 (4 years ago)

Market Day Krabbycakes recall

Recalled by Market Day Local Inc. · Whitefish, MT, United States

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

Why it was recalled

Undeclared shrimp and carmine color

Undeclared allergen: Shellfish

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

Market Day Krabbycakes, Item 3320, Net Wt. 40 oz. (2.5 lbs.) 1.13kg. Item Number 803320R. UPC 51497 14360. Light panko Breadcrumbs blended with Snow Crab meat, Fresh Cream & Real Butter with Seasonings. Keep Frozen - Fully Cooked. Distributed & Sold exclusively by: Market Day Local, Inc. Whitefish, MT 59937

Quantity: 840 bags

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.

Product with a Best By date of 05/10/2023 and earlier.

Where it was sold

California Georgia Illinois Indiana Kansas Kentucky Maryland Michigan Missouri North Carolina New Jersey Ohio Pennsylvania Virginia Wisconsin

FDA's distribution note: CA, GA, IL, IN, KS, KY, MD, MI, MO, NC, NJ, OH, PA, HC, VA, WI

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 shellfish; 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
Market Day Local Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
May 13, 2022
In FDA report of
Jul 20, 2022
Terminated
Aug 20, 2025
FDA recall number
F-1417-2022 · event 90193
Official record
FDA enforcement report search