CLASS I Food recall · Reported 2 Apr 2014 · FDA Enforcement Report

Kinnikinnick Original Homestyle Waffles Cardboard recalled

World Pure Foods Wholesalers is recalling Kinnikinnick Original Homestyle Waffles Cardboard, distributed in Michigan. The recall was initiated on 13 Jan 2014 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBB 20131209, 20131231, BB 2014 0126, 2014 AL15, 2014 JN24, 2014 JL29
Quantity recalled39 cases

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-1694-2014
FDA event ID
67602
Recalling firm
World Pure Foods Wholesalers, Dearborn, MI
Classification
Class I
Status
Terminated
Recall initiated
13 Jan 2014
FDA classified
25 Mar 2014
Reported
2 Apr 2014
Type
Voluntary: Firm initiated
Customers notified by
FAX
Reason category
Undeclared Milk
Product category
Other

Timeline

13 Jan 2014Recall initiated by company
25 Mar 2014Classified by FDA+71 days
2 Apr 2014Published in enforcement report+8 days

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

Reason for recall

Undeclared milk

Product as listed by the FDA

Kinnikinnick Original Homestyle Waffles 210 g/7.4 oz Cardboard Box UPC 620133001981

Where it was distributed

retail stores in Michigan

Michigan

Questions about this recall

Why was it recalled?

Undeclared milk

Which lots are affected?

BB 20131209, 20131231, BB 2014 0126, 2014 AL15, 2014 JN24, 2014 JL29

Where was it sold?

retail stores in Michigan

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 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

2 other products · FDA event 67602

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