CLASS II Food recall · Reported 9 Jul 2014 · FDA Enforcement Report

Number One Sompa Salted Fish recalled by Lao Thai Nam

Lao Thai Nam is recalling Lao Thai Nam Number One Sompa Salted Fish, distributed in Texas. The recall was initiated on 31 Mar 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll product distributed prior to 03/31/14.
Quantity recalled120 packs

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-2057-2014
FDA event ID
67864
Recalling firm
Lao Thai Nam, Dallas, TX
Brand
Lao
Classification
Class II
Status
Terminated
Recall initiated
31 Mar 2014
FDA classified
27 Jun 2014
Reported
9 Jul 2014
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Botulism
Product category
Fish

Timeline

31 Mar 2014Recall initiated by company
27 Jun 2014Classified by FDA+88 days
9 Jul 2014Published 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

The product has the potential to be contaminated with Clostridium botulinum.

Product as listed by the FDA

Lao Thai Nam Number One Sompa Salted Fish, Net Wt 7 oz. (198 g), Produced by Lao Thai Nam, 4444 W. Illinois Ave., Ste 400a, Dallas, TX 75211, UPC 8 84332 00019 4

Where it was distributed

TX

Texas

Questions about this recall

Is Number One Sompa Salted Fish recalled?

Yes. Lao Thai Nam recalled Number One Sompa Salted Fish on 31 Mar 2014. The recall is Class II and its status is Terminated. Recall number F-2057-2014.

Why was it recalled?

The product has the potential to be contaminated with Clostridium botulinum.

Which lots are affected?

All product distributed prior to 03/31/14.

Where was it sold?

TX

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 21 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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