Beaver Brand Tartar Sauce with Fresh Capers and Dill
Reason Undeclared soy in Tartar sauce. Ingredients statement declares soybean oil.
Inglehoffer Seafood Tartar Sauce With Lemon & Capers recall
Recalled by Beaverton Foods Inc · Hillsboro, OR, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Undeclared soy in Tartar sauce. Ingredients statement declares soybean oil.
Undeclared allergen: Soy
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
Inglehoffer Seafood Tartar Sauce With Lemon & Capers, 8.25oz (234g) jar, UPC 0 71828 01114 1. The label is read in parts: "***Inglehoffer*** Seafood TARTAR SAUCE WITH LEMON & CAPERS*** INGREDIENTS: SOYBEAN OIL, WATER, CUCUMBERS, EGGS, WHITE DISTILLED VINEGAR, SALT, MUSTARD SEED, LEMON JUICE, HIGH FRUCTOSE CORN SYRUP, ONIONS, CORN SYRUP, SUGAR, XANTHAN GUM, SPICES, NATURAL FLAVORS, PRESERVATIVES ***Packed by Beaverton Foods Inc. ***".
Quantity: 140 cases (6/8.25 oz jars per case)
Food: 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.
Best By Date OCT 29 2022. Lot # Z302405. Lot code breakdown: First digit Z = Year Identifier 2021, following digits 302 = Julian Date of Manufacture (10/29/2021), 4 = Line 4 where it was packed and 05 = the sequence on the production schedule.
Where it was sold
Oregon South Carolina
FDA's distribution note: Distributors in two states: OR and SC.
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern.
- Recalling firm
- Beaverton Foods Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 21, 2021
- In FDA report of
- Feb 2, 2022
- FDA recall number
- F-0521-2022 · event 89273
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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