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Stavis Seafoods, Inc. Recall: Product may contain elevated levels of histamine. - F-2232-2019

United States

TerminatedClass II

Company
Stavis Seafoods, Inc.
Product
MiCal brand YELLOWFIN TUNA POKE CUBE, Raw, Frozen, Product o…
Recall date
September 9, 2019
Terminated
December 19, 2019
Source
FDA

Reason for recall

Product may contain elevated levels of histamine.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
MiCal brand YELLOWFIN TUNA POKE CUBE, Raw, Frozen, Product of Vietnam, Wild Caught. Cube size - 1 inch (2cm x 2cm) AAA grade. Product is packed in 1lb vacuum packed bags in a pre-printed labeled master case. Master case weight is 5lbs. Not published in this source record 1,330lbs or 133 cases Production Date: 04 20 2019; Expiration Date: 04 19 2021

Distribution

  • Products were distributed in NY
  • OH
  • MI
  • PA
  • MD
  • NJ
  • MA
  • NC

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-2232-2019
Event ID
83756
Status
Terminated
Classification
Class II
Company
Stavis Seafoods, Inc.
Product description
MiCal brand YELLOWFIN TUNA POKE CUBE, Raw, Frozen, Product of Vietnam, Wild Caught. Cube size - 1 inch (2cm x 2cm) AAA grade. Product is packed in 1lb vacuum packed bags in a pre-printed labeled master case. Master case weight is 5lbs.
Quantity
1,330lbs or 133 cases
Reason
Product may contain elevated levels of histamine.
Recall initiation date
September 9, 2019
Report date
September 25, 2019
Classification date
Not published in this source record
Termination date
December 19, 2019
Distribution pattern
Products were distributed in NY,OH,MI,PA,MD,NJ,MA, NC
UPC, lot, and code information
Production Date: 04 20 2019; Expiration Date: 04 19 2021
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Stavis Seafoods, Inc.

Other recalls from Stavis Seafoods, Inc.

FDA Recall United States TerminatedTerminated: October 10, 2018Historical recordClass III

Stavis Seafoods, Inc.

Product
Ocean Delight Individually Vacuum Packed AHI TUNA SAKU, 8-12…
Published
August 15, 2018
Distribution
NH, MA, NY, ME, RI, CT, MO, OH, NC, MI,…

View recall →

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
Ohio 1
Michigan 1
Pennsylvania 1
Maryland 1
New Jersey 1
Massachusetts 1
North Carolina 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.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

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 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 December 19, 2019.

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.

View the official FDA source

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.

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