Food Recall Check
Class II · Moderate risk Terminated Initiated Apr 10, 2019 (7 years ago)

Trader Joe's Saucy Scallops with Mushrooms recall

Recalled by Frial SAS · St Martin Des Entrees, N/A, France

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Scallop flavor used in the product contains low levels of crustaceans (1 ppm) that is not listed on the product label.

Undeclared allergen: Shellfish

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Trader Joe's Saucy Scallops with Mushrooms, NET Wt. 16 oz. (1 LB) 454 g UPC 0093 0390 24 units per case Product of France Dist. and sold exclusively by: Trader Joe's Monrovia, CA 91016

Quantity: unknown

Food: Seafood & fish

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

18024 18037 18043 18058 18074 18082 18088 18103 18115 18156 18187 18199 18207 18240 18298 18327 19025 19032 19070 19101

Where it was sold

Alaska Arkansas Hawaii Mississippi Montana South Dakota West Virginia Wyoming

FDA's distribution note: All US states EXCEPT Alaska, Arkansas, Hawaii, Mississippi, Montana, South Dakota, West Virginia and Wyoming.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to shellfish; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Frial SAS
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 10, 2019
In FDA report of
May 8, 2019
Terminated
Aug 30, 2019
FDA recall number
F-1316-2019 · event 82634
Official record
FDA enforcement report search

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