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CriticalFDAfda-F-1153-2017LISTERIA

Refrigerated, Ready to Eat Herring in Brine, Herring Fillet "Matjes" sold under the FRESH SEAFOOD label, packaged in plastic retail con...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
10
Recall Date
December 2, 2016
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1153-2017.

The product has the potential to be contaminated with Listeria monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1153-2017.

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 Royal Seafood Baza, 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-1153-2017.

Royal Seafood Baza, 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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Royal Seafood Baza, Inc. Recall FAQ

Royal Seafood Baza, Inc. is the subject of a seafood safety report: Refrigerated, Ready to Eat Herring in Brine, Herring Fillet "Matjes" sold under the FRESH SEAFOOD label, packaged in plastic retail con.... The notice was published on December 2, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 10 units are potentially affected.