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Stavis Seafoods, Inc. Recall: Product is decomposed. - F-1755-2018

United States

TerminatedClass III

Company
Stavis Seafoods, Inc.
Product
Ocean Delight Individually Vacuum Packed AHI TUNA SAKU, 8-12…
Recall date
July 18, 2018
Terminated
October 10, 2018
Source
FDA

Reason for recall

Product is decomposed.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Ocean Delight Individually Vacuum Packed AHI TUNA SAKU, 8-12 oz. NET WT. 10 LB (4.54 kg) and 12-16 oz. NET WT. 22LB (9.98 kg), Carbon Monoxide Treated, DISTRIBUTED BY: Stavis Seafoods, WILD CAUGHT, PRODUCT OF SRI LANKA Not published in this source record 10 lb. = 2960 lbs. & 22 lb. = 1584 lbs. 8 - 12 oz. / 10 LB (4.54 kg) - Lot # 85599 Production Code - 11018 UPC Code - GTIN (01)00091372680013(11)180411(422)144(10)01 Production Code - 11088 UPC Code - GTIN (01)00091372680013(11)180418(422)144(10)01 12 - 16 oz. / 22 LB (9.98 kg) - Lot #85598 Production Code - 11098 UPC Code - GTIN (01)00091372680006(11)180419(422)144(10)01

Distribution

  • NH
  • MA
  • NY
  • ME
  • RI
  • CT
  • MO
  • OH
  • NC
  • MI
  • PA
  • MN
  • & PR.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1755-2018
Event ID
80560
Status
Terminated
Classification
Class III
Company
Stavis Seafoods, Inc.
Product description
Ocean Delight Individually Vacuum Packed AHI TUNA SAKU, 8-12 oz. NET WT. 10 LB (4.54 kg) and 12-16 oz. NET WT. 22LB (9.98 kg), Carbon Monoxide Treated, DISTRIBUTED BY: Stavis Seafoods, WILD CAUGHT, PRODUCT OF SRI LANKA
Quantity
10 lb. = 2960 lbs. & 22 lb. = 1584 lbs.
Reason
Product is decomposed.
Recall initiation date
July 18, 2018
Report date
August 15, 2018
Classification date
Not published in this source record
Termination date
October 10, 2018
Distribution pattern
NH, MA, NY, ME, RI, CT, MO, OH, NC, MI, PA, MN, & PR.
UPC, lot, and code information
8 - 12 oz. / 10 LB (4.54 kg) - Lot # 85599 Production Code - 11018 UPC Code - GTIN (01)00091372680013(11)180411(422)144(10)01 Production Code - 11088 UPC Code - GTIN (01)00091372680013(11)180418(422)144(10)01 12 - 16 oz. / 22 LB (9.98 kg) - Lot #85598 Production Code - 11098 UPC Code - GTIN (01)00091372680006(11)180419(422)144(10)01
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: December 19, 2019Historical recordClass II

Stavis Seafoods, Inc.

Product
MiCal brand YELLOWFIN TUNA POKE CUBE, Raw, Frozen, Product o…
Published
September 25, 2019
Distribution
Products were distributed in NY,OH,MI,PA…

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 Hampshire 1
Massachusetts 1
New York 1
Maine 1
Rhode Island 1
Connecticut 1
Missouri 1
Ohio 1
North Carolina 1
Michigan 1
Pennsylvania 1
Minnesota 1
Puerto Rico 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 III mean?

FDA classifies this recall as Class III. 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 October 10, 2018.

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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