FDA recall record

Jensens Old Fashioned Smokehouse Low salt, vacuum packaged, Hot Smoked Salmon recall — FDA F-1391-2014

Jensen's Old Fashioned Smokehouse, Inc. is recalling Lusamerica, Jensen's and ALCHEMIST SEAFOODs Hot Smoked Salmon products may not labeled "KEEP FROZEN"…

Class IIclassification
F-1391-2014official record ID
Jan 22, 2014report date

Recall record at a glance

Official recordF-1391-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmJensens Old Fashioned Smokehouse Inc.
Report dateJan 22, 2014
Recall initiation dateApr 29, 2013
Quantity14,628 lbs
LocationSeattle, WA, United States

Official product description

Low salt, vacuum packaged, Hot Smoked Salmon (may include any of the following varieties Coho, Keta, King, Sockeye). Jensen's product is labeled in part "*** JENSEN'S SEATTLE STYLE SMOKED WILD PACIFIC SALMON JENESN'S SMOKEHOUSE, INC. *** Keep Refrigerated Below 38 F*** INGREDIENTS: WILD PACIFIC KING SALMON, SALT, BROWN SUGAR, HARDWOOD SMOKE ***" Lusamerica Keta or Sockey product is shipped with the "Keep Frozen" sticker on individual units. No label was provided. ALCHEMIST SEAFOOD King or Coho product is labeled parts: "***Get Wild ALCHEMIST SEAFOODS***wwww.AlchemistSeafoods.com Wild Alaskan Salmon***INGREDIENTS (smoked product): Wild Alaskan Salmon, Salt, Brown Sugar, Natural Wood Smoke***Thaw Under Refrigeration Just Prior to Consumption***Product of Alaska, U.S.A.***.

Why the product was recalled

Jensen's Old Fashioned Smokehouse, Inc. is recalling Lusamerica, Jensen's and ALCHEMIST SEAFOODs Hot Smoked Salmon products may not labeled "KEEP FROZEN" and products are potentially contaminated with Clostridium botulinum.

Distribution information

Distributed in Washington

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

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