CLASS I Food recall · Reported 6 Mar 2013 · FDA Enforcement Report
Bream Dry Salted Fish recalled by Zip International Group
Zip International Group is recalling Bream Dry Salted Fish, distributed in New York. The recall was initiated on 7 Feb 2013 and the FDA has classified it as Class I.
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-1007-2013
- FDA event ID
- 64337
- Recalling firm
- Zip International Group, Edison, NJ
- Brand
- Bream Dry
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 7 Feb 2013
- FDA classified
- 25 Feb 2013
- Reported
- 6 Mar 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Product category
- Fish
Timeline
| 7 Feb 2013 | Recall initiated by company | |
| 25 Feb 2013 | Classified by FDA | +18 days |
| 6 Mar 2013 | 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
NYSDAM sampling and analysis has revealed that Dry Salted Fish is uneviscerated.
Product as listed by the FDA
Bream Dry Salted Fish Net Wt.: about 14.2 oz Imported by Zip International Group LLC Product of Russia
Where it was distributed
NY
Questions about this recall
Is Bream Dry Salted Fish recalled?
Yes. Zip International Group recalled Bream Dry Salted Fish on 7 Feb 2013. The recall is Class I and its status is Terminated. Recall number F-1007-2013.
Why was it recalled?
NYSDAM sampling and analysis has revealed that Dry Salted Fish is uneviscerated.
Which lots are affected?
835856001228; sell by 03/27/2013
Where was it sold?
NY
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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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