Odyssey Enterprises Inc Recall: Cooked King crab legs & claws were recalled due to a contamination with Listeria monocytogenes.

🇺🇸 United States

1. August 1, 2016 - Recall initiated
2. September 14, 2016 - Reported by source
3. September 8, 2016 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2037-2016

Status

Terminated

Classification

Class II

Company

Odyssey Enterprises Inc

Product description

Split Cooked King Crab Leg & Claw, repacked by Odyssey, net wt. 20 lbs. per box, keep frozen. UPC 28575 96323 The label is read in parts: "***SPLIT COOKED KING CRAB LEG & CLAW***PRODUCT OF RUSSIA***PACKED IN U.S.A. ***NET WT. 20 LBS***KEEP FROZEN***PACKED FOR: ODYSSEY BY: NORTHWEST SEAFOOD PROCESSORS INC***206 SW Michigan ST Seattle, WA 98106***FURTHER PREPARATION BEFORE SERVING AS FOLLOWS: FROM FROZEN STATE BOIL, STEAM OR BROIL FOR 8-10 MINUTES OR BAKE IN 400F OVEN FOR 8-10 MINUTES***".

Quantity

Not published in this source record

Reason

Cooked King crab legs & claws were recalled due to a contamination with Listeria monocytogenes.

Recall initiation date

August 1, 2016

Report date

September 14, 2016

Classification date

Not published in this source record

Termination date

September 8, 2016

Distribution pattern

distributed in WI

UPC, lot, and code information

Not published in this source record

Voluntary or mandated

Not published in this source record

Initial notification method

Not published in this source record

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Odyssey Enterprises Inc

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Wisconsin	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

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: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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.

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