CLASS III Food recall · Reported 20 Apr 2016 · FDA Enforcement Report

Waveland Pancake and Waffle Mix recalled by Heartland Products

Heartland Products is recalling Waveland Pancake and Waffle Mix, 030608, distributed in Iowa, Illinois. The recall was initiated on 27 Aug 2015 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesNo lot number given; date of manufacture was 6/4/2015
Quantity recalled48 - 25 lb. boxes

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-1080-2016
FDA event ID
71942
Recalling firm
Heartland Products, Des Moines, IA
Classification
Class III
Status
Terminated
Recall initiated
27 Aug 2015
FDA classified
13 Apr 2016
Reported
20 Apr 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Other

Timeline

27 Aug 2015Recall initiated by company
13 Apr 2016Classified by FDA+230 days
20 Apr 2016Published in enforcement report+7 days

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

Reason for recall

Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Waveland Pancake and Waffle Mix, 030608, packaged in 25-lb. poly-lined cardboard boxes, Manufactured Heartland Products, Inc. Des Moines, IA 50321.

Where it was distributed

Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.

IowaIllinois

Questions about this recall

Why was it recalled?

Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.

Which lots are affected?

No lot number given; date of manufacture was 6/4/2015

Where was it sold?

Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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

5 other products · FDA event 71942

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