CLASS II Food recall · Reported 7 Oct 2020 · FDA Enforcement Report

Brownie, Chocolate Brownie and Vanilla Ice Cream Sammich recalled

Shatto Milk is recalling Brownie, Chocolate Brownie and Vanilla Ice Cream Sammich. The recall was initiated on 9 Sep 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesExpiration 11/20/2020
Quantity recalled308 sandwiches

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0003-2021
FDA event ID
86418
Recalling firm
Shatto Milk, Osborn, MO
Brand
Brownie
Classification
Class II
Status
Terminated
Recall initiated
9 Sep 2020
FDA classified
1 Oct 2020
Reported
7 Oct 2020
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Soy

Timeline

9 Sep 2020Recall initiated by company
1 Oct 2020Classified by FDA+22 days
7 Oct 2020Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The firm was informed by their supplier than an ingredient in the cookie portion of their ice cream sandwiches contain the undeclared major food allergen soy (soy lecithin)

Product as listed by the FDA

Shatto Milk Company, Brownie, Chocolate Brownie and Vanilla Ice Cream Sammich, Net Wt. 5 oz, Shatto Milk Company, Osborn, MO

Where it was distributed

Grocery stores in the Kansas City metro area.

Questions about this recall

Why was it recalled?

The firm was informed by their supplier than an ingredient in the cookie portion of their ice cream sandwiches contain the undeclared major food allergen soy (soy lecithin)

Which lots are affected?

Expiration 11/20/2020

Where was it sold?

Grocery stores in the Kansas City metro area.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 86418

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