CLASS II ONGOING Food recall · Reported 1 Mar 2017 · FDA Enforcement Report

Sunmba Frozen Ajiaco (Vegetable Mix) recalled by Barberi International

Barberi International is recalling Sunmba Frozen Ajiaco (Vegetable Mix), distributed in Florida. The recall was initiated on 25 Jan 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot code 10516, Exp. Nov 5, 2017
Quantity recalled1,440 units

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-1482-2017
FDA event ID
76336
Recalling firm
Barberi International, Miami, FL
Brand
Sunmba
Classification
Class II
Status
Ongoing
Recall initiated
25 Jan 2017
FDA classified
17 Feb 2017
Reported
1 Mar 2017
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Listeria
Product category
Other

Timeline

25 Jan 2017Recall initiated by company
17 Feb 2017Classified by FDA+23 days
1 Mar 2017Published 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

Contamination with Listeria monocytogenes

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Sunmba Frozen Ajiaco (Vegetable Mix), 2 lbs.

Where it was distributed

Distributed throughout Florida

Florida

Questions about this recall

Why was it recalled?

Contamination with Listeria monocytogenes

Which lots are affected?

Lot code 10516, Exp. Nov 5, 2017

Where was it sold?

Distributed throughout Florida

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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