CT Concerns recalls Fresh Wild Tuna (delivered in white styrofoam boxes) due to potential Listeria monocytogenes contamination from FDA swab tests. No finished packaging; produced May 27-28, 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.
CT Concerns is recalling Fresh Wild Tuna that was delivered to restaurants in white styrofoam boxes without finished packaging. This recall is due to potential Listeria monocytogenes contamination found in FDA environmental swab tests.
FDA environmental swab tests detected Listeria monocytogenes, a bacteria that can cause serious foodborne illness. The recall is initiated because the tuna was potentially contaminated during handling or storage.
Restaurant customers who received the tuna in white styrofoam boxes from CT Concerns between May 27-28, 2014. People who ate the tuna after this date may be at risk.
Check for Fresh Wild Tuna delivered to restaurants in white styrofoam boxes without finished packaging. The product was produced between May 27 and May 28, 2014.
Look for Fresh Wild Tuna delivered in white styrofoam boxes without finished packaging, produced between May 27 and May 28, 2014.
The recall is due to potential Listeria monocytogenes contamination found in FDA swab tests, so it is not safe to eat.
Check for Fresh Wild Tuna delivered to restaurants in white styrofoam boxes without finished packaging, produced between May 27 and May 28, 2014.
The official recall notice does not specify actions for those who have consumed the product.
We’ve drafted a message you can send CT Concerns to request your refund or repair — edit it as you like.
Subject: Recall F-2420-2014 — CT Concerns CT Concerns Hello, I own a CT Concerns that is covered by recall F-2420-2014 from CT Concerns. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
