CLASS III Food recall · Reported 20 Mar 2013 · FDA Enforcement Report
Tausi Salted Black Beans recalled by JMT Trading Company
JMT Trading is recalling Tausi Salted Black Beans, distributed in California, Hawaii. The recall was initiated on 10 Jan 2013 and the FDA has classified it as Class III.
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-1130-2013
- FDA event ID
- 64156
- Recalling firm
- JMT Trading, South San Francisco, CA
- Brand
- Tausi
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 10 Jan 2013
- FDA classified
- 13 Mar 2013
- Reported
- 20 Mar 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Other Reasons
- Product category
- Candy
Timeline
| 10 Jan 2013 | Recall initiated by company | |
| 13 Mar 2013 | Classified by FDA | +62 days |
| 20 Mar 2013 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Reports were received of swollen cans of Tausi Salted Black Beans imported from the Philippines.
Product as listed by the FDA
Tausi Salted Black Beans, 180 gram (6.34 oz.) can. Ingredient: Black Beans, Water, Iodized salt, sugar and caramel. Distributed by V8 Commercial Co., Inc., San Juan, Metro Manila. Product of the Philippines. UPC 97399 00109
Where it was distributed
CA Bay area and one location in HI.
Questions about this recall
Why was it recalled?
Reports were received of swollen cans of Tausi Salted Black Beans imported from the Philippines.
Which lots are affected?
BB:FEB.15, 2013; BB:APR.26, 2013; BB:FEB 15, 2014; BB: APR.11,2013.
Where was it sold?
CA Bay area and one location in HI.
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 III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
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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