RecallHawk
Class I Recall

Haddock, Monkfish, Bone-in Trout, Grouper, Red Snapper, Red Rock Cod, Ocean Perch, Pacific Cod, Halibut, Coho Salmon, At

Northeast Seafood Products, Incorporated

Summary

The FDA issued a Class I for Haddock, Monkfish, Bone-in Trout, Grouper, Red Snapper, Red Rock Cod, Ocean Perc by Northeast Seafood Products, Incorporated. Reason: Seafood and fin fish products potentially contaminated with Salmonella and implicated in illness outbreak.

Details

Source

Food Recall

External ID

F-0158-2022

Action Date

2021-11-10

Status

Terminated

Category

food

Product Description

Haddock, Monkfish, Bone-in Trout, Grouper, Red Snapper, Red Rock Cod, Ocean Perch, Pacific Cod, Halibut, Coho Salmon, Atlantic Salmon Portions, Lane Snapper, Tilapia, All Natural Salmon Fillet, Pacific Sole, and Farm Raised Striped Bass

Lot/Code Info: Production/distribution dates from May 2021 to October 7, 2021.

Quantity Affected: 6416.49 lbs.

Reason for Recall

Seafood and fin fish products potentially contaminated with Salmonella and implicated in illness outbreak

Distribution

Restaurants and grocery stores in Colorado

Type: Voluntary: Firm initiated

Recall Initiated: 2021-10-07

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 54 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Northeast Seafood Products, Incorporated) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Northeast Seafood Products, Incorporated have FDA actions?

This is the only FDA action we have on record for Northeast Seafood Products, Incorporated in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0158-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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