Food Recall Check
Class II · Moderate risk Terminated Initiated Nov 11, 2022 (4 years ago)

Sardines in tomato sauce packed in cans labeled in part recall

Recalled by St. Jean's Coast Mountain Resources Ltd. (dba) St. Jean's Ca · Nanaimo, N/A, Canada

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

Why it was recalled

Canned sardines in tomato sauce recalled due to high levels of histamine.

Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.

What was recalled

Sardines in tomato sauce packed in cans labeled in part, "WILD PACIFIC SARDINES RAINCOAST TRADING TM***IN TOMATO SAUCE***NET. 4.2 oz (120 g)***INGREDIENTS: SARDINES, WATER, TOMATO PASTE, SEA SALT. PRODUCT OF MALAYSIA PACKED FOR: RAINCOAST TRADING, NANAIMO, BC CANADA V9R6Z5***8 10757 00917 7***BEST BEFORE 19 JUL 2024***"

Quantity: 195 cases

Food: Seafood & fish Sauces, dips & dressings

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.

Product UPC 8 10757 00917 7 with BEST BEFORE 19 JUL 2024. Manufactured 19 JUL 2021. Stock code 966025PEY-USOB12

Where it was sold

Arizona California Idaho Montana Oregon Washington

FDA's distribution note: Distributed wholesale to 148 retail customers in AZ, CA, ID, MT, OR, WA.

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. 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
St. Jean's Coast Mountain Resources Ltd. (dba) St. Jean's Ca
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 11, 2022
In FDA report of
Dec 21, 2022
Terminated
May 11, 2023
FDA recall number
F-0195-2023 · event 91191
Official record
FDA enforcement report search

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