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

Z Tejas Cornbread Blend recalled by C. H. Guenther & Son

C. H. Guenther & Son is recalling Z Tejas Cornbread Blend 212759, distributed nationwide in the US. The recall was initiated on 7 Dec 2015 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesAll lots
Quantity recalled424 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-0866-2016
FDA event ID
72822
Recalling firm
C. H. Guenther & Son, Denton, TX
Brand
Z Tejas
Classification
Class III
Status
Terminated
Recall initiated
7 Dec 2015
FDA classified
11 Apr 2016
Reported
20 Apr 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Foreign Material
Product category
Other

Timeline

7 Dec 2015Recall initiated by company
11 Apr 2016Classified by FDA+126 days
20 Apr 2016Published 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

May contain small metal fragments from wire mesh sifter.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Z Tejas Cornbread Blend 212759 NET WEIGHT 4.5 LBS. (2.04 kg)

Where it was distributed

Nationwide throughout the US

Nationwide

Questions about this recall

Is Z Tejas Cornbread Blend 212759 recalled?

Yes. C. H. Guenther & Son recalled Z Tejas Cornbread Blend 212759 on 7 Dec 2015. The recall is Class III and its status is Terminated. Recall number F-0866-2016.

Why was it recalled?

May contain small metal fragments from wire mesh sifter.

Which lots are affected?

All lots

Where was it sold?

Nationwide throughout the 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 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 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.

More recalls from C. H. Guenther & Son

All 84

Other Other recalls

All 4,664