FDA recall record

Orca Bay Foods Trader Joe's brand Gluten Free Battered Halibut, SKU 00503822 recall — FDA F-0117-2021

Undeclared Wheat and Milk.

Class Iclassification
F-0117-2021official record ID
Nov 25, 2020report date

Recall record at a glance

Official recordF-0117-2021
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmOrca Bay Foods LLC
Report dateNov 25, 2020
Recall initiation dateOct 23, 2020
Quantity356 cases
LocationSeattle, WA, United States

Official product description

Trader Joe's brand Gluten Free Battered Halibut, SKU 00503822. Product of USA. Frozen product is packed in plastic bag and sold in retail carton box (10 oz. box). Each master case contains 20/10 oz. boxes. RETAIL BOX'S label is read in parts: '***TRADER JOE'S BATTERED HALIBUT GLUTEN FREE ***INGREDIENTS: HALIBUT, WATER, YELLOW CORN FLOUR, MODIFIED CORN STARCH, RICE FLOUR, SALT, ONION POWDER, GARLIC POWDER, LEAVENING (SODIUM BECARNONATE, SODIUM ACID PYROPHOSPHATE), XANTHAN GYUM,, GUAR GUM, CANOLA OIL*** CONTAINS HALIBUT *** WILD CAUGHT PRODUCT OF USA ***KEEP FROZEN***00503822". MASTER CASE label is correctly declared as ""***Trader Joe's Lightly Battered Halibut ***ALLERGENS: HALIBUT (FISH), WHEAT, MILK***SKU 00269803***".

Why the product was recalled

Undeclared Wheat and Milk.

Distribution information

Distributed in Connecticut, Illinois, Indiana, Iowa, Kansas, Kentucky, Maine, Massachusetts, Michigan, Minnesota, Missouri, Nebraska, New Hampshire, New York, Ohio, Rhode Island, Tennessee, Vermont, and Wisconsin.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

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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