Food Recall Check
Class II · Moderate risk Terminated Initiated Aug 21, 2020 (6 years ago)

Schaws Sweet and Sassy Gourmet Barbecue and Basting Sauce recall

Recalled by Lac O' Seasons Resort,Inc · Iron River, MI, United States

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

Why it was recalled

Undeclared allergens (Soy and Anchovies)

Undeclared allergens: Soy Fish

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

SCHAWS SWEET AND SASSY GOURMET BARBECUE AND BASTING SAUCE, 18oz glass jar, UPC code 6 90379 81241

Quantity: Approximately 9112 units (total)

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.

All jars with a use by date of 8/20/2022 and prior

Where it was sold

Michigan

FDA's distribution note: Schaws Sauce is distributed primarily in Michigan, but it is also retailed through the company web site, schawssauce.com

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 soy, fish; 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
Lac O' Seasons Resort,Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 21, 2020
In FDA report of
Sep 16, 2020
Terminated
Oct 16, 2020
FDA recall number
F-1426-2020 · event 86320
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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