St. James Smokehouse, Scotch Reserve, Scottish Smoked Salmon, Net Wt 4oz (114g)
Summary
The FDA issued a Class I for St. James Smokehouse, Scotch Reserve, Scottish Smoked Salmon, Net Wt 4oz (114g) by St. James Smokehouse, Inc.. Reason: Possible contamination with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-1809-2022
Action Date
2022-10-05
Status
Terminated
Category
food
Product Description
St. James Smokehouse, Scotch Reserve, Scottish Smoked Salmon, Net Wt 4oz (114g)
Lot/Code Info: Lot #123172, Batch #6550
Quantity Affected: 11,141 x 4oz packs of Scotch Reserve Scottish Smoked Salmon
Reason for Recall
Possible contamination with Listeria monocytogenes
Distribution
16 domestic consignees and 1 international: MALABAR FARMS FOOD SERVICE LTD CARAPO VILLAGE. ARIMA. TRINIDAD. W.I . Tel: 868 642 6329
Type: Voluntary: Firm initiated
Recall Initiated: 2022-08-26
Company
Miami, FL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 76 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (St. James Smokehouse, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does St. James Smokehouse, Inc. have FDA actions?
This is the only FDA action we have on record for St. James Smokehouse, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1809-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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