CLASS I Food recall · Reported 11 Mar 2026 · FDA Enforcement Report

Lobster & Crab Ravioli recalled by Perfect Pasta, Incorporated

Perfect Pasta, Incorporated is recalling Lobster & Crab Ravioli, distributed in Utah. The recall was initiated on 8 Feb 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesMade on: JAN 19 2026
Quantity recalled42/ 10 lb cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0620-2026
FDA event ID
98425
Recalling firm
Perfect Pasta, Incorporated, West Valley City, UT
Brand
Lobster
Classification
Class I
Status
Terminated
Recall initiated
8 Feb 2026
FDA classified
24 Mar 2026
Reported
11 Mar 2026
Type
Voluntary: Firm initiated
Customers notified by
Visit
Product category
Milk

Timeline

8 Feb 2026Recall initiated by company
11 Mar 2026Published in enforcement report+31 days
24 Mar 2026Classified by FDA+13 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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.

Where it was distributed

Distributed to consignees in Utah only.

Utah

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Made on: JAN 19 2026

Where was it sold?

Distributed to consignees in Utah only.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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