Food Recall Check
Class I · High risk Terminated Initiated Apr 14, 2022 (4 years ago)

Mio Salad Dressing packaged in recall

Recalled by Joonsung Trading Inc · Portland, OR, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared egg. Label declares Mayo but does not declare Egg.

Undeclared allergen: Egg

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

Mio Salad Dressing packaged in 1 gallon plastic jug. Label read in parts: "Ingredient: Onion, Carrot, Ginger water, Soybean oil, Reg. Vinegar, Mayo, Sushi Ginger".

Quantity: 15 - 1 gallon containers

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.

The product with a date prior to APR 14 2022 is recalled.

Where it was sold

Oregon Washington

FDA's distribution note: Distributed in Oregon and Washington

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; 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
Joonsung Trading Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 14, 2022
In FDA report of
Jun 1, 2022
Terminated
Jun 14, 2022
FDA recall number
F-1078-2022 · event 90040
Official record
FDA enforcement report search

Also recalled with it (4 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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