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Class II: temporary or reversible health riskTerminated

AJC International Early Dawn Recall

Early Dawn

AJC International, Inc. · Atlanta, GA

Risk level
Class II
Reported by FDA
Jan 10, 2018
Recall ID
F-0563-2018
Check your lot numberHow we source this data

Summary

AJC International recalled Early Dawn starting Dec 22, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0563-2018 on Jan 10, 2018. Reason: Early Dawn Whole Tilapia was sampled and found positive for the antibiotic, Sulfadiazine. Status: Terminated.

Why it was recalled

Early Dawn Whole Tilapia was sampled and found positive for the antibiotic, Sulfadiazine.

Product description

Early Dawn; Whole Tilapia IQF, Gutted & Scaled, Farm Raised, 40 lbs.; Size 550-750g OR 750g+, Lot No.: 1985507; Production Date: 08/12/2017; Best Used By Date: 02/12/2019; Product of China.

Lot numbers, UPCs & expiration codes

Lot No.: 1985507; Production Date: 08/12/2017; Best Used By Date: 02/12/2019

Where it was sold

PA

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0563-2018
Classification
Class II
Status
Terminated
Recall initiated
Dec 22, 2017
FDA report date
Jan 10, 2018
Quantity
169 cases
Recall type
Voluntary: Firm initiated
Recalling firm
AJC International, Inc.

Original FDA data

Every field from FDA enforcement report F-0563-2018, exactly as published.

Show all FDA fields
City
Atlanta
State
GA
Status
Terminated
Country
United States
Event ID
78829
Address
1000 Abernathy Rd Ste 600
Code information
Lot No.: 1985507; Production Date: 08/12/2017; Best Used By Date: 02/12/2019
Postal code
30328-5647
Report date
Jan 10, 2018
Product type
Food
Recall number
F-0563-2018
Classification
Class II
Recalling firm
AJC International, Inc.
Product quantity
169 cases
Termination date
Apr 27, 2020
Reason for recall
Early Dawn Whole Tilapia was sampled and found positive for the antibiotic, Sulfadiazine.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Early Dawn; Whole Tilapia IQF, Gutted & Scaled, Farm Raised, 40 lbs.; Size 550-750g OR 750g+, Lot No.: 1985507; Production Date: 08/12/2017; Best Used By Date: 02/12/2019; Product of China.
Distribution pattern
PA
Recall initiation date
Dec 22, 2017
Initial firm notification
E-Mail
Center classification date
Jan 10, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0563-2018, published Jan 10, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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