Cold-Smoked Atlantic Salmon in vacuum packed plastic, labeled in part: "FOPPEN NORWEGIAN SMOKED SALMON SLICES INCLUDES PACKET OF HONEY MUSTARD DILL SAUCE READY TO EAT PEPPERED TRADITIONAL DILL NET WT 12oz / 341g (291g Salmon + 50g Sauce 8 712224 129277***INGREDIENTS SALMON: Atlantic Salmon (Salmo salar), salt, pepper, dill, paprika, parsley, smoke, color added***Manufactured by: Foppen Salmon Daltonstraat 24, 3846 BX HARDERWIJK, The Netherlands***"
Class I - DangerousWhat Should You Do?
- Check if you have this product: Expiration dates between 10.1.12 - 10.27.12.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Costco Wholesale
- Reason for Recall:
- Salmon was produced in a plant in Greece, owned by Foppen of the Netherlands, where Salmonella was found on one of the lines.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Cold-Smoked Atlantic Salmon in vacuum packed plastic, labeled in part: "FOPPEN NORWEGIAN SMOKED SALMON SLICES INCLUDES PACKET OF HONEY MUSTARD DILL SAUCE READY TO EAT PEPPERED TRADITIONAL DILL NET WT 12oz / 341g (291g Salmon + 50g Sauce 8 712224 129277***INGREDIENTS SALMON: Atlantic Salmon (Salmo salar), salt, pepper, dill, paprika, parsley, smoke, color added***Manufactured by: Foppen Salmon Daltonstraat 24, 3846 BX HARDERWIJK, The Netherlands***"
Product Codes/Lot Numbers:
Expiration dates between 10.1.12 - 10.27.12.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0823-2013
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