Food Recall Check
Class I · High risk Terminated Initiated Feb 8, 2026 (8 months ago)

Lobster & Crab Ravioli recall

Recalled by Perfect Pasta, Incorporated · West Valley City, UT, United States

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

Why it was recalled

Undeclared shrimp, crab, lobster, pollock (fish), whiting (fish), and soy.

Undeclared allergens: Soy Fish 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

Lobster & Crab Ravioli. Keep Frozen. Contains: Wheat, Eggs, Milk, Crustaceans-Shellfish. Product is intended to be further cooked. Weight: 1-10 pound (4.5g). Use within 6 months. 801-541-9292-www.FunarosPerfectPasta.com. 1391 So. 300 West Slc, Ut 84115.

Quantity: 42/ 10 lb cases

Food: Seafood & fish

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.

Made on: JAN 19 2026

Where it was sold

Utah

FDA's distribution note: Distributed to consignees in Utah only.

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. The risk from an undeclared allergen is to people allergic to soy, fish, 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
Perfect Pasta, Incorporated
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 8, 2026
In FDA report of
Mar 11, 2026
Terminated
Mar 27, 2026
FDA recall number
H-0620-2026 · event 98425
Official record
FDA enforcement report search

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