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Perfect Pasta, Incorporated Recall: Undeclared shrimp, crab, lobster, pollock (fish), whiting (fish), and soy.

United States

TerminatedClass I

Company
Perfect Pasta, Incorporated
Product
Lobster & Crab Ravioli. Keep Frozen. Contains: Wheat, Eggs,…
Recall date
February 8, 2026
Terminated
March 27, 2026
Source
FDA

Reason for recall

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

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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. Not published in this source record 42/ 10 lb cases Made on: JAN 19 2026

Distribution

  • Distributed to consignees in Utah only.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0620-2026
Event ID
98425
Status
Terminated
Classification
Class I
Company
Perfect Pasta, Incorporated
Product description
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
Reason
Undeclared shrimp, crab, lobster, pollock (fish), whiting (fish), and soy.
Recall initiation date
February 8, 2026
Report date
March 11, 2026
Classification date
Not published in this source record
Termination date
March 27, 2026
Distribution pattern
Distributed to consignees in Utah only.
UPC, lot, and code information
Made on: JAN 19 2026
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Perfect Pasta, Incorporated

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.