CLASS II Food recall · Reported 2 Oct 2013 · FDA Enforcement Report

Meijer Carrot Uniced Split Cake Layers (product is recalled

Maplehurst Bakeries is recalling Meijer Carrot Uniced Split Cake Layers (product is, distributed in Michigan, Ohio. The recall was initiated on 10 Sep 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSKU: 00569, Lot Codes: 3221G00569, 3221H00569, 3221I00569 Shelf life (Exp. Date): Best if Used Before: 2/5/2014
Quantity recalled1561 cases with 24 cakes/case (37464 individual cakes)

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-1912-2013
FDA event ID
66271
Recalling firm
Maplehurst Bakeries, Brownsburg, IN
Brand
Meijer
Classification
Class II
Status
Terminated
Recall initiated
10 Sep 2013
FDA classified
23 Sep 2013
Reported
2 Oct 2013
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Foreign Material
Product category
Cakes & Pastries

Timeline

10 Sep 2013Recall initiated by company
23 Sep 2013Classified by FDA+13 days
2 Oct 2013Published 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

Product was found to contain foreign material, flexible plastic.

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

Meijer 8 Inch Carrot Uniced Split Cake Layers (product is packed in bulk cartons of 24 units/paper bags lined with flexible blue plastic liner).

Where it was distributed

MI and OH.

MichiganOhio

Stores named: Meijer

Questions about this recall

Is Meijer Carrot Uniced Split Cake Layers (product is recalled?

Yes. Maplehurst Bakeries recalled Meijer Carrot Uniced Split Cake Layers (product is on 10 Sep 2013. The recall is Class II and its status is Terminated. Recall number F-1912-2013.

Why was it recalled?

Product was found to contain foreign material, flexible plastic.

Which lots are affected?

SKU: 00569, Lot Codes: 3221G00569, 3221H00569, 3221I00569 Shelf life (Exp. Date): Best if Used Before: 2/5/2014

Where was it sold?

MI and OH.

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 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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