CLASS III Food recall · Reported 17 Oct 2012 · FDA Enforcement Report

Frozen IQF PND Shrimp (Farm Raised), size 61/70 recalled

Chang Jiang Seafood Ca is recalling Frozen IQF PND Shrimp (Farm Raised), size 61/70 and size 71/90 (6bgsx5lbs), distributed in Arizona, California, Utah. The recall was initiated on 27 Aug 2012 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesProduct has no lot numbers. Product date: 15-11-2011.
Quantity recalled719 cartons

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-0025-2013
FDA event ID
63182
Recalling firm
Chang Jiang Seafood Ca, South El Monte, CA
Classification
Class III
Status
Terminated
Recall initiated
27 Aug 2012
FDA classified
5 Oct 2012
Reported
17 Oct 2012
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Shrimp

Timeline

27 Aug 2012Recall initiated by company
5 Oct 2012Classified by FDA+39 days
17 Oct 2012Published 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

Chang Jiang Seafood CA Inc. is recalling Frozen Shrimp because it contains nitrofuran which is an unapproved antibiotic.

Product as listed by the FDA

Frozen IQF PND Shrimp (Farm Raised), size 61/70 and size 71/90, 30 lbs (6bgsx5lbs)

Where it was distributed

AZ, CA, UT

ArizonaCaliforniaUtah

Questions about this recall

Why was it recalled?

Chang Jiang Seafood CA Inc. is recalling Frozen Shrimp because it contains nitrofuran which is an unapproved antibiotic.

Which lots are affected?

Product has no lot numbers. Product date: 15-11-2011.

Where was it sold?

AZ, CA, UT

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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