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Unisea Inc. Recall: Shrimp Burgers are recalled because the Ingredients statement declared butter, shrimp, cod, and/or Pollock but the Contains statement declared only fish & shellfish.

United States

TerminatedClass II

Company
Unisea Inc.
Product
Frozen Wild Shrimp Burgers, Wild Grill Foods brand, net wt.…
Recall date
April 28, 2017
Terminated
July 31, 2017
Source
FDA

Reason for recall

Shrimp Burgers are recalled because the Ingredients statement declared butter, shrimp, cod, and/or Pollock but the Contains statement declared only fish & shellfish.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Frozen Wild Shrimp Burgers, Wild Grill Foods brand, net wt. 12 oz. Each package contains 4/ 3 oz. pieces. UPC 8 94067 00248 6. The 12 oz. package label is read in parts: "***SHRIMP BURGERS***WILD GRILL***Net WT WT. 12 OZ.***Distributed by Wild Grill Foods***INGREDIENTS: Shrimp, Cod and or Pollock, Butter, Gluten Free Panko (Rice Flour, Xanthan Gum, Evaporated Cane Sugar, Yeast, Sea Salt, Ascorbic Acid), Scallions, Contains 2% or less of Shallots, Garlic, Parsley, Spices, Sea Salt***CONTAINS: Fish, Shellfish***". The master case's label is read in parts: "***Item #44100***Contains: 12/ 4x3 oz. Units Distributed By: Wild Grill Foods PO Box 21301 Eugene, OR 97402***Perishable. Keep Frozen at 0F***". Not published in this source record 208 cases (12/12 oz. Packages per case) Lot # 5302A. Best By: January 18, 2017. Lot # 6174A. Best By: June 21, 2017. Lot # 6259A. Best By: September 23, 2017.

Distribution

  • distributed in CA
  • OR
  • PA
  • and WA.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-2185-2017
Event ID
77158
Status
Terminated
Classification
Class II
Company
Unisea Inc.
Product description
Frozen Wild Shrimp Burgers, Wild Grill Foods brand, net wt. 12 oz. Each package contains 4/ 3 oz. pieces. UPC 8 94067 00248 6. The 12 oz. package label is read in parts: "***SHRIMP BURGERS***WILD GRILL***Net WT WT. 12 OZ.***Distributed by Wild Grill Foods***INGREDIENTS: Shrimp, Cod and or Pollock, Butter, Gluten Free Panko (Rice Flour, Xanthan Gum, Evaporated Cane Sugar, Yeast, Sea Salt, Ascorbic Acid), Scallions, Contains 2% or less of Shallots, Garlic, Parsley, Spices, Sea Salt***CONTAINS: Fish, Shellfish***". The master case's label is read in parts: "***Item #44100***Contains: 12/ 4x3 oz. Units Distributed By: Wild Grill Foods PO Box 21301 Eugene, OR 97402***Perishable. Keep Frozen at 0F***".
Quantity
208 cases (12/12 oz. Packages per case)
Reason
Shrimp Burgers are recalled because the Ingredients statement declared butter, shrimp, cod, and/or Pollock but the Contains statement declared only fish & shellfish.
Recall initiation date
April 28, 2017
Report date
May 17, 2017
Classification date
Not published in this source record
Termination date
July 31, 2017
Distribution pattern
distributed in CA, OR, PA, and WA.
UPC, lot, and code information
Lot # 5302A. Best By: January 18, 2017. Lot # 6174A. Best By: June 21, 2017. Lot # 6259A. Best By: September 23, 2017.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Unisea Inc.

Distribution map

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

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
California 1
Oregon 1
Pennsylvania 1
Washington 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:

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.