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Capital Street LLC Recall: NYSDAM sampling and analysis has determined that Lake Fresh Smoked Tilapia is un-evsicerated.

United States

TerminatedClass I

Company
Capital Street LLC
Product
Lake Fresh Whole Smoked Tilapia Net Wt 8 oz Capital Street…
Recall date
March 4, 2017
Terminated
February 22, 2019
Source
FDA

Reason for recall

NYSDAM sampling and analysis has determined that Lake Fresh Smoked Tilapia is un-evsicerated.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Lake Fresh Whole Smoked Tilapia Net Wt 8 oz Capital Street LLC Old Bridge, NJ 08857 UPC 0680296079 0680296079 4 boxes - 20, 1/2 lb packs per box Lot SM0616-01 June 21 2017

Distribution

  • NY

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1886-2017
Event ID
76651
Status
Terminated
Classification
Class I
Company
Capital Street LLC
Product description
Lake Fresh Whole Smoked Tilapia Net Wt 8 oz Capital Street LLC Old Bridge, NJ 08857 UPC 0680296079
Quantity
4 boxes - 20, 1/2 lb packs per box
Reason
NYSDAM sampling and analysis has determined that Lake Fresh Smoked Tilapia is un-evsicerated.
Recall initiation date
March 4, 2017
Report date
April 19, 2017
Classification date
Not published in this source record
Termination date
February 22, 2019
Distribution pattern
NY
UPC, lot, and code information
UPC 0680296079; Lot SM0616-01 June 21 2017
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Letter
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Capital Street LLC

Distribution map

A map highlighting the states named in the source's distribution description.

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
New York 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.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

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. Read the full medical disclaimer.