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CriticalFDAfda-F-1804-2015CONTAMINATION

Hellas Golden Double Smoked Herring Vacuum Karagounis Bros SA -Hellas -35 A.3 - C.E. 2nd Industrial Zone -37500 VOLOS TEL.: +30 24250...

⚠ Critical Alert — Stop Using Immediately

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

Category
Units Affected
1,650
Recall Date
February 11, 2015
Issuing Agency
Hazard
Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1804-2015.

Smoked herring may be potentially contaminated with C. botulinum.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1804-2015.

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 Moscahlades Bros 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-1804-2015.

Moscahlades Bros 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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Moscahlades Bros Inc Recall FAQ

Moscahlades Bros Inc is the subject of a food safety report: Hellas Golden Double Smoked Herring Vacuum Karagounis Bros SA -Hellas -35 A.3 - C.E. 2nd Industrial Zone -37500 VOLOS TEL.: +30 24250.... The notice was published on February 11, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 1,650 units are potentially affected.