CLASS I Food recall · Reported 1 Aug 2012 · FDA Enforcement Report

Vanilla Maple, 1pt recalled by Arctic Zero

Arctic Zero is recalling Vanilla Maple, 1pt, distributed nationwide in the US. The recall was initiated on 6 Jul 2012 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesProduction dates 1/1/11 - 2/29/12
Quantity recalled2,303,112 units of pints total

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-1776-2012
FDA event ID
51819
Recalling firm
Arctic Zero, Escondido, CA
Classification
Class I
Status
Terminated
Recall initiated
6 Jul 2012
FDA classified
23 Jul 2012
Reported
1 Aug 2012
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Undeclared Milk
Product category
Other

Timeline

6 Jul 2012Recall initiated by company
23 Jul 2012Classified by FDA+17 days
1 Aug 2012Published in enforcement report+9 days

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

Reason for recall

Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.

Product as listed by the FDA

Vanilla Maple, 1pt., UPC 8 52244 00306 0

Where it was distributed

Nationwide in US

Nationwide

Questions about this recall

Is Vanilla Maple, 1pt recalled?

Yes. Arctic Zero recalled Vanilla Maple, 1pt on 6 Jul 2012. The recall is Class I and its status is Terminated. Recall number F-1776-2012.

Why was it recalled?

Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.

Which lots are affected?

Production dates 1/1/11 - 2/29/12

Where was it sold?

Nationwide in US

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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