Inglehoffer Seafood Tartar Sauce With Lemon & Capers, 8.25oz (234g) jar, UPC 0 71828 01114 1. The label is read in pa
Summary
The FDA issued a Class III for Inglehoffer Seafood Tartar Sauce With Lemon & Capers, 8.25oz (234g) jar, UPC 0 by Beaverton Foods Inc. Reason: Undeclared soy in Tartar sauce. Ingredients statement declares soybean oil..
Details
Source
Food Recall
External ID
F-0521-2022
Action Date
2022-02-02
Status
Ongoing
Category
food
Product Description
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. ***".
Lot/Code Info: 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.
Quantity Affected: 140 cases (6/8.25 oz jars per case)
Reason for Recall
Undeclared soy in Tartar sauce. Ingredients statement declares soybean oil.
Distribution
Distributors in two states: OR and SC.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-12-21
Company
Hillsboro, OR
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 117 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Beaverton Foods Inc has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Beaverton Foods Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Beaverton Foods Inc have FDA actions?
Beaverton Foods Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0521-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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