FDA recall record

Northwest Gourmet Food Products New England Clam Chowder, Pike Place Chowder brand, item recall — FDA F-0528-2020

The outer retail packaging claims "Gluten Free" but the inner individual pouch declares wheat.

Class IIclassification
F-0528-2020official record ID
Jan 29, 2020report date

Recall record at a glance

Official recordF-0528-2020
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNorthwest Gourmet Food Products Inc.
Report dateJan 29, 2020
Recall initiation dateDec 18, 2019
QuantityNew England Clam Chowder = 190 cases.
LocationRenton, WA, United States

Official product description

New England Clam Chowder, Pike Place Chowder brand, item #89200, distributed By PPC Trading Co. M. BOX #262 4580 Klahanie Drive SE Issaquah WA 98029. There are 12/16 oz. retail packages per master case. Retail package net wt. 16 oz. UPC 8 56112 00402 9. The 16 oz. inner individual pouch has a clear film lid and the label is read in parts: "***Pike Place CHOWDER ***NEW ENGLAND CLAM CHOWDER *** CONTAINS: FISH (COD), MILK, SOY, WHEAT***". The outer RETAIL package, which house the 16 oz. inner individual pouch, is read in parts: "***Pike Place CHOWDER *** NEW ENGLAND CLAM CHOWDER *** Highest Quality Clams. Farm Fresh Ingredients. Pure Cream & Butter ***THAWING INSTRUCTIONS***COOKING INSTRUCTIONS ***Allergens: Fish, Shellfish, Milk, Soy***GLUTEN FREE***". The MASTER case label is read in parts: "*** PIKE PLACE CHOWDER *** NEW ENGLAND CLAM CHOWDER ***89200 ***KEEP FROZEN UNTIL USED. THAW UNDER REFRIGERATION IMMEDIATELY BEFORE USE*** PRODUCT MAY BE KEPT UNDER REFRIGERATION FOR UP TO 15 DAYS PRIOR TO USE *** CONTAINS: FISH (COD), MILK, SOY, WHEAT***".

Why the product was recalled

The outer retail packaging claims "Gluten Free" but the inner individual pouch declares wheat.

Distribution information

distributed in CO and WA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

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