CLASS II Food recall · Reported 8 Jun 2022 · FDA Enforcement Report

Dawson Food Products Belgian Style Waffle Mix recalled

Dorothy Dawson Food Products is recalling Dawson Food Products Belgian Style Waffle Mix, distributed in Michigan. The recall was initiated on 6 May 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes04142022B1
Quantity recalled14 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-1102-2022
FDA event ID
90223
Recalling firm
Dorothy Dawson Food Products, Jackson, MI
Brand
Dawson
Classification
Class II
Status
Terminated
Recall initiated
6 May 2022
FDA classified
1 Jun 2022
Reported
8 Jun 2022
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
E. coli
Product category
Fish

Timeline

6 May 2022Recall initiated by company
1 Jun 2022Classified by FDA+26 days
8 Jun 2022Published 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

Product tested over specification for coliforms and positive for low levels of E.coli

Some strains of E. coli, such as O157:H7, produce a toxin that can cause severe stomach cramps, bloody diarrhea and, in a small number of cases, kidney failure.

Product as listed by the FDA

Dawson Food Products Belgian Style Waffle Mix, 5 lbs. bag, bag UPC 758162120844, item code D6000A0; 6, 5 lbs. bags per case

Where it was distributed

MI

Michigan

Questions about this recall

Why was it recalled?

Product tested over specification for coliforms and positive for low levels of E.coli

Which lots are affected?

04142022B1

Where was it sold?

MI

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.

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