Northern Fisheries Ltd. Recall: Products have the potential to cause scombrotoxin fish poisoning because they may have increased levels of histamine. - F-0461-2020
🇺🇸 United States
TerminatedClass II
Company
Northern Fisheries Ltd.
Product
Frozen Yellowfin Tuna Steak, 4 oz. and 6 oz., Keep Frozen, I…
Recall date
December 6, 2019
Terminated
June 12, 2020
Source
FDA
Reason for recall
Products have the potential to cause scombrotoxin fish poisoning because they may have increased levels of histamine.
- Recall initiated
- Reported by source
- Recall terminated
Recalled products
Product description
UPC
Quantity
Lot / code information
Frozen Yellowfin Tuna Steak, 4 oz. and 6 oz., Keep Frozen, Imported/Distributed: Mical Seafood Inc., 10400 Griffin Rd, Suite #209, Cooper City, Florida 33328
Not published in this source record
1,052 cases
all 2019 production dates codes
Distribution
Distributors in 5 states: FL
GA
NY
IL and RI
Official source record
Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0461-2020
Event ID
84440
Status
Terminated
Classification
Class II
Company
Northern Fisheries Ltd.
Product description
Frozen Yellowfin Tuna Steak, 4 oz. and 6 oz., Keep Frozen, Imported/Distributed: Mical Seafood Inc., 10400 Griffin Rd, Suite #209, Cooper City, Florida 33328
Quantity
1,052 cases
Reason
Products have the potential to cause scombrotoxin fish poisoning because they may have increased levels of histamine.
Recall initiation date
December 6, 2019
Report date
January 1, 2020
Classification date
Not published in this source record
Termination date
June 12, 2020
Distribution pattern
Distributors in 5 states: FL, GA, NY, IL and RI
UPC, lot, and code information
all 2019 production dates codes
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 84440 with 2 other product
entries in Public Health Trace.
FDA Recall🇺🇸 United StatesTerminatedTerminated: June 12, 2020Historical recordClass II
A map highlighting the states named in the source's distribution description.
Distributed
No data published
Shading reflects state-level totals only, as published by the source. It does not imply
county-level or point-level precision.
Distribution map
State
Distributed
Florida
1
Georgia
1
New York
1
Illinois
1
Rhode Island
1
States shown are extracted from the source's free-text distribution description above; a narrative
description (e.g. "distributed nationwide") may not list individual states to extract.
View raw source data
-- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for
current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of June 12, 2020.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company
or product is unsafe beyond what the official source has published.
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