CLASS II Food recall · Reported 15 Mar 2023 · FDA Enforcement Report

Elsa kolo Yegbes Kolo Belewez recalled by Ebenezer Ethio Market

Ebenezer Ethio Market is recalling Elsa kolo Yegbes Kolo Belewez, distributed in Minnesota. The recall was initiated on 12 Dec 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesNo Code on product.
Quantity recalled550-500 kg

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-0401-2023
FDA event ID
91525
Recalling firm
Ebenezer Ethio Market, Burnsville, MN
Brand
Elsa
Classification
Class II
Status
Terminated
Recall initiated
12 Dec 2022
FDA classified
3 Mar 2023
Reported
15 Mar 2023
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Mold
Product category
Other

Timeline

12 Dec 2022Recall initiated by company
3 Mar 2023Classified by FDA+81 days
15 Mar 2023Published in enforcement report+12 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 not properly labeled in English for importing into the US and filth was found in product (including mold, hair, bird feather, yarn).

Product as listed by the FDA

Elsa kolo Yegbes Kolo Belewez

Where it was distributed

MN

Minnesota

Questions about this recall

Why was it recalled?

Product was not properly labeled in English for importing into the US and filth was found in product (including mold, hair, bird feather, yarn).

Which lots are affected?

No Code on product.

Where was it sold?

MN

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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