Re: Inquiry on canned tuna quality

From: Ko, Iwan Setiyono (isk025@student.uit.no)
Date: Sun May 29 2005 - 10:07:24 PDT

  • Next message: Ko, Iwan Setiyono: "PART 2 : Inquiry on canned tuna quality"

    Hi again,

    Thanks for the information but do you mind to share with me about these
    points:

    1. Has anybody observed/analyzed the histamine level of the same can code,
    lot, same product of canned tuna products at, at least, TWO different time
    stamps?

    Say product SJOC (Skipjack Chunk in sunflower oil) can code SUSUMU

    First grading in the lab
    The above product was graded on July 17, 2000 (after incubation - for
    example: 7 days after production date) and the histamine content is 15
    ppm.

    Second grading in the lab
    The same product graded on July 17, 2003 (i.e. 3 years after the 1st
    grading). Is the histamine content higher than that of the 1st one? For
    example, it is now become 23 ppm? If it is not always higher, can we say
    that older can age TENDS to have HIGHER histamine level?

    or in other words,
    2. Older can age (3, 4 or even 5 years after production date - considering
    that, in general, canned tuna product designed to have 5-year shelf-life)
    tend to have higher histamine levels?

    3. Can you explain why after retorting, people are so concern about
    recontamination of the product when they are still hot out of retort
    tube(they said that forklift or improper handling during this stage may
    introduce contamination). How? Is it because the swelling of the can due
    to the heat creates small openings between the seam?

    Anyone interested to supervise me? :)

    -- 
    Kindly regards,
    

    Ko, Iwan Setiyono (Ko, I.S.) MSc Candidate - International Fisheries Management Norwegian College of Fishery Science (NFH) University of Tromsų - Breivika N-9037 Tromsų NORWAY Mobile: +47 4500 4097 E-mail: isk025@student.uit.no

    Angel M Suarez said: > > Whenever an FDA inspector at the port of entry sample for canned tuna > this is send to the laboratory for decomposition and histamine analysis. > If the product is found to be decomposed or with histamine levels then > this entry is detained under Import Alert 16-105. The FDA import alert > 16-105 for canned tuna states that canned tuna is subject to refusal of > admission in the United States because after sampling and testing it > appears to bear or contain histamine, a poisonous and deleterious > substance in such quantity as ordinarily renders it injurious to health. > This is considered adulteration, under Section 402(a)(1)] of the Food > Drug and Cosmetic Act. > > There are other ways FDA may find out canned tuna could have histamine > this is through a consumer complaint. The complainant had a reaction due > to consumption of the product analysis test positive for histamine. FDA > probably will perform examination of future entries and if histamine is > found then the product is detained. > > The manufacturing firm must have a HACCP plan that has a Critical > Control Point that prevents histamine formation during receiving and > process. Chapter 7 of the Fish and Fisheries Products Hazards and > Controls Guide, Third Edition, states that scombrotoxin formation is a > the result of time/tempera abuse of certain species of fish that can > cause consumer illness. > > In addition to sampling canned tuna for histamine analysis the FDA can > detain canned product found injurious to health based on any of the > following: > a) The manufacturing firm failed to register under 21 CFR 108 for all > manufacturer that process low acid canned food products thermally > process under 21 CFR 113 or acidified food 21 CFR 114. > b) FDA field examination at port of entry detected that cans were > abnormal with defects such as swelling, springer, flippers, seam defects > that are critical that may result in the loss of the hermetic seal. > c) The manufacturing firm is under detention because is under Import > Alert 99-04, Detention Without Physical Examination of Manufacturer for > Low Acid Canned Food and Acidified products because the firm failed to > respond to verify information, failure to verify process, inadequate pH, > inadequate process. > d) Field examination detected that cans were mislabeled such as foreign > language, no information country of origin, > e) Failure by the manufacturer register under the Bioterrorism Act > f) Failure to submit prior notice at the port of entry. > > Hope this answer and provide you guidance. > > Angel M. Suarez, > Registered Sanitarian > Ceti > 7865 Thor Drive > Annandale, VA 22003-1437 > Tel/FAX 703-560-4499 > E-mail: cetifish@verizon.net > > > > Ko, Iwan Setiyono wrote: > >>Dear all, >>I am interested to study canned tuna quality and need some assistance. >>Anybody would like to explain these following questions? >> >>1. Based on your experience, do you think the reject products when they >>are under US FDA detention do tend come from older can age (3, 4 or even >> 5 >>years old) after production date? >> >>2. Do you think it's mainly due to the histamine content? Or other >>microbiological problems? >> >>3. How do you generally assess the quality of the canned product of >>increasing can age compared with the newly produced one, based on >>chemical, microbiological and sensory criteria? >> >>Looking forward to hearing it from you. >> >> >> > > -- > > >



    This archive was generated by hypermail 2b29 : Sun May 29 2005 - 10:08:59 PDT