CLASS II Food recall · Reported 9 Jul 2014 · FDA Enforcement Report
Yangban Rice Porridge with Abalone recalled by Hk Galleria Wholesale L.p
HK Galleria Wholesale is recalling Yangban Rice Porridge with Abalone, distributed in California. The recall was initiated on 29 Apr 2014 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-5060-2014
- FDA event ID
- 68160
- Recalling firm
- HK Galleria Wholesale, Los Angeles, CA
- Brand
- Yangban
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 29 Apr 2014
- FDA classified
- 30 Jun 2014
- Reported
- 9 Jul 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Botulism
- Product category
- Rice
Timeline
| 29 Apr 2014 | Recall initiated by company | |
| 30 Jun 2014 | Classified by FDA | +62 days |
| 9 Jul 2014 | Published 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
HK Galleria Wholesale is recalling Rice Porridge with Abalone because it may be contaminated with Clostridium botulinum.
Product as listed by the FDA
Yangban Rice Porridge with Abalone, Net Wt. 10.16 oz (288 g), UPC 8 83298 61617 3, 24 cans/case
Where it was distributed
California
Questions about this recall
Why was it recalled?
HK Galleria Wholesale is recalling Rice Porridge with Abalone because it may be contaminated with Clostridium botulinum.
Which lots are affected?
Lot#: 2015-01-24
Where was it sold?
California
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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