FDA recall record

Ocean Beauty Seafoods Cold-smoked salmon in vacuum plastic bags that are partially recall — FDA F-0913-2013

Ocean Beauty Seafood's sample was found positive for Listeria monocytogenes.

Class Iclassification
F-0913-2013official record ID
Jan 23, 2013report date

Recall record at a glance

Official recordF-0913-2013
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmOcean Beauty Seafoods, LLC
Report dateJan 23, 2013
Recall initiation dateDec 13, 2012
Quantity272 cases - 12/3 ounce packages per case. The press release had reported 275 cases had been distributed, but that was incorrect.
LocationSeattle, WA, United States

Official product description

Cold-smoked salmon in vacuum plastic bags that are partially clear and partially colored black, white, gold and pink. Nathan's, 3oz Nova Salmon, has the UPC 0 73030 80368 2. The front panel is labeled in part: "***NATHAN'S TRADITIONAL DELICATESSEN NOVA SALMON CLASSIC SMOKED***NET WT 3 OZ (85g)***" back panel: "***NATHAN'S TRADITIONAL DELICATESSEN NOVA SALMON CLASSIC SMOKED***This salmon can be frozen for up to 45 days. Thaw under refrigeration. Once opened, keep refrigerated and be sure to enjoy within five days. Keep refrigerated at 38F or below.***0 73030 80368 2***INGREDIENTS: ATLANTIC SALMON (COLOR ADDED), SALT, SUGAR, PRESERVATIVES (SODIUM BENZOATE, SODIUM ERYTHORBATE, SODIUM NITRITE), FD&C YELLOW #5, YELLOW #6, RED #40, BLUE #1, AND NATURAL HARDWOOD SMOKE. DISTRIBUTED BY OCEAN BEAUTY SEAFOODS LLC, SEATTLE, WA 98119 WWW.OCEANBEAUTY.COM FARM RAISED PRODUCT OF CHILE***." A white stick-on label, affixed to the top left hand corner of the back panel, reads: top line: "***M228208***;" middle line left to right: "***07 09 285 12 14 09***;" and bottom line: "***10632***."

Why the product was recalled

Ocean Beauty Seafood's sample was found positive for Listeria monocytogenes.

Distribution information

Nationwide to distributors and retailers in AZ, CA, CO, CT, MA, NH, NJ, NY, OR, PA, RI, TX and WA.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

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About this record

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