FDA recall record

California Shellfish, Inc. dba Hallmark Ocean Supreme and Yaquina Bay IQF shrimp meat recall — FDA F-1535-2019

The product was recalled because there was a foreign object found inside product packaging.

Class IIclassification
F-1535-2019official record ID
Jul 17, 2019report date

Recall record at a glance

Official recordF-1535-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCalifornia Shellfish, Inc. dba Hallmark Fisheries
Report dateJul 17, 2019
Recall initiation dateJun 14, 2019
Quantity46,585 lbs.
LocationCharleston, OR, United States

Official product description

Ocean Supreme and Yaquina Bay IQF shrimp meat, product of USA wild caught, cooked and peeled, 5 lb. bag, 4/5 lb. bags per box, net wt. 20#. The BAG label is read in parts: "***Ocean Supreme *** Cooked & Peeled I.Q.F SHRIMP MEAT ***Ingredients: Shrimp Meat and Salt ***Net Wt. 5 lbs. *** Packed By Hallmark Fisheries, Charleston, Oregon*** Wild Caught Product of U.S.A *** CFN-3018852***". The CASE label is read in parts: "***Ocean Supreme *** COOKED AND PEELED IQF SHRIMP MEAT ***INGREDIENTS: SHRIMP MEAT *** AND SALT*** PRODUCT OF U.S.A. WILD CAUGHT***". The BAG label is read in parts: "***YAQUINA BAY*** Cooked & Peeled I.Q.F SHRIMP MEAT ***Ingredients: Shrimp Meat and Salt ***Net Wt. 5 lbs. *** Packed By Hallmark Fisheries, Charleston, Oregon*** Wild Caught Product of U.S.A *** CFN-3018852***" The CASE label is read in parts: "***Yaquina Bay *** COOKED AND PEELED IQF SHRIMP MEAT ***INGREDIENTS: SHRIMP MEAT *** AND SALT*** PRODUCT OF U.S.A. WILD CAUGHT***"

Why the product was recalled

The product was recalled because there was a foreign object found inside product packaging.

Distribution information

distributed in CA, OR, and WA and in Canada.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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