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High RiskFDAfda-F-2419-2014LISTERIA

Fresh Atlantic Salmon. No finished packaging. Fresh Salmon is placed in white styrofoam box and delivered to area restaurants.

Category
Units Affected
1,590
Recall Date
June 19, 2014
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2419-2014.

Firm is initiating a voluntary recall of Fresh Farmed Atlantic Salmon and Fresh Wild Tuna because it has the potential to be contaminated with Listeria monocytogenes. Firm was notified that FDA environmental swab samples had a positive result for Listeria monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2419-2014.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Ct Concerns, Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2419-2014.

CT Concerns, Inc.

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Ct Concerns, Inc. Recall FAQ

Ct Concerns, Inc. is the subject of a seafood safety report: Fresh Atlantic Salmon. No finished packaging. Fresh Salmon is placed in white styrofoam box and delivered to area restaurants.. The notice was published on June 19, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 1,590 units are potentially affected.