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