Food recall: Misty Fjord Lemon Pepper Smoked Salmon, vacuum sealed 6 oz plastic packs.
Misty Fjord Seafood LLC (Winthrop, WA) initiated this food recall on 21 Apr 2016; FDA lists 3 product records under event 73962, classified Class II.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 43% of the 799 food enforcement events initiated in 2016 carry the same class.
Status: Terminated, terminated 8 Nov 2016. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Misty Fjord Seafood LLC.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Misty Fjord Seafood LLC, Winthrop, WA.
Reason for recall
"Misty Fjord Seafoods LLC is recalling Lemon Pepper smoked salmon, Maple smoked salmon and Lox salmon due to the potential to be contaminated with Listeria Monocytogenes."
Distribution
"unknown at this time"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0348-2017 | Misty Fjord Lemon Pepper Smoked Salmon, vacuum sealed 6 oz plastic packs. | — | Class II | Terminated | 16 Nov 2016 |
| F-0349-2017 | Misty Fjord Maple Smoked Salmon, vacuum sealed 6 oz plastic packs. | — | Class II | Terminated | 16 Nov 2016 |
| F-0350-2017 | Misty Fjord Lox, vacuum packed in 4 oz serving size packs. | — | Class II | Terminated | 16 Nov 2016 |
Context
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Misty Fjord Seafoods LLC is recalling Lemon Pepper smoked salmon, Maple smoked salmon and Lox salmon due to the potential to be contaminated with Listeria Monocytogenes."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "unknown at this time"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 8 Nov 2016. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.