Slaughter 2 Flashcards
What does the EU health mark signify?
That food has been produced to current standards of hygienic food production in licensed premises and allows food to be traced back to those premises
On what products is the EU health mark required?
All animal products for human consumption e.g. milk
What information is included on the EU health mark?
- Country
- Producer
- European Community (EC)
Outline the Third Country approval procedure
- National authority submits formal request
- Must include: type of animal/product, anticipated volume of trade, main importing EU countries, class of animals, description of minimum treatment, number and type of establishments considered to meet EU requirements
- Questionnaire sent to and filled out by National Authority
- Bilateral contracts between NA and Commission
- On the spot inspection organised with FVO
- Report of inspection sent to NA, Commission, EU parliament, Member States
- Draft legislation to add 3d country
- Proposed legislation adopted by Commission
What is the purpose of Third Country approval for imports
Ensure animal products imported have been produced under the same legislation and to the same standard as in EU countries
Who has the responsibility for the health, welfare and food hygiene in the slaughterhouse?
The processing company
What is the Clean Livestock Policy?
- Policy that applies to sheep and cattle
- Ensures farmer has the responsibility to bring only clean and dry animals to slaughter
What happens to animals that are identified as not fit for slaughter on AMI?
Are killed but disposed of as ABP
What are the requirements regarding slaughter of TB reactors?
- Must be sent to specific approved slaughterhouses
- Following their slaughter need to clean and disinfect the processing area
- Place at end of processing line
Outline the responsibilities of the FBO
- Ensure all animals presented to OV
- Ensure only healthy animals accepted for human slaughter
- Identification of animals (match to passports and FCI)
Why can animals that are DOA not enter the human food chain?
No AMI was carried out
What are the requirements to enable animals to be accepted into the slaughterhouse?
- Proper ID
- Accompanied by relevant information
- No movement restrictions (unless permitted by Competent Authority)
- Clean and healthy
- Satisfactory welfare
What must be done if requirements for entry into slaughterhouse are not met?
- FBO must notify OV
- Use isolation facilities for suspect animals
What are the roles of the OV in the slaughterhouse?
- Verify FBO compliance
- AMI
- PMI in certain conditions
How is cleanliness of animals assessed in slaughterhouses?
- Visual inspection
- Categorised 1-5
Describe the appearance and consequences for a category 1 cleanliness animal
- Dry, clean with regard to dung/dirt
- Very minor amounts of loosely adherent straw/bedding
- Accepted for slaughter without any special treatment
Describe the appearance and consequences for a category 2 cleanliness animal
- Slightly dirty, dry/damp
- Light contamination with dirt/dung
- Small amounts of loosely adherent straw/bedding
- Accepted for slaughter without special treatment
Describe the appearance and consequences for a category 3 cleanliness animal
- Dirty
- Dry/damp
- Significant contamination with dirt/dung
- Significant amounts of adherent straw/bedding
- rejected for slaughter except in exceptional circumstances e.g. animal welfare grounds, disease control reasons
Describe the appearance and consequences for a category 4 cleanliness animal
- Very dirty
- Dry/damp
- Heavily contaminated with dirt/dung
- Significant amounts of adherent bedding
- Should not enter production line
- Rejected for slaughter except in exceptional circumstances e.g. animal welfare disease control reasons
- May have procedures in place to allow slaughter e.g. placing last in slaughter line, slow line to allow staff cleaning between animals, minimise splashing
Describe the appearance and consequences for a category 5 cleanliness animal
- Filthy, wet
- Very heavy contamination with dirt/dung
- Lots of adherent bedding
- Rejected for slaughter, should not be unloaded and sent back to farm, should not have been sent to slaughter
What are the aims of AMI?
- Establish fitness for human consumption
- Notifiable disease surveillance
- Animal welfare monitoring
What happens if notifiable disease or welfare issue on farm is suspected?
APHA informed
What happens if welfare issue during transport is suspected?
Trading Standards Agency informed
What is required by the OV in order to carry out the AMI effectively?
- Light
- Space
- Facilities
- Assistance
- Time
- Proper equipment (PPE, torch, thermometer, stethoscope)
Give examples of notifiable diseases that may be identified on AMI in cattle
- Anthrax
- Aujeszky’s
- BSE
- Bluetongue
- Brucellosis
- Enzootic bovine leukosis
- FMD
- Lumpy skin disease
- Rift valley fever
- Rinderpest
- bTB
- Vesicular stomatitis
- Warble fly
Outline the considerations when pneumonia is suspected on AMI
- In cow: discharge from nostrils, foaming at mouth
- Some respiratory distress
- Should not have been transported
- Withdrawal period from drugs a concern
- Emaciation may occur with systemic disease
- May have had special certification to allow travel
- First in line to minimise standing time
Outline the considerations following finding of ringworm on AMI
- Common in cattle
- Only an issue as potential zoonotic infection via contact
- Nothing of major concern on AMI
Outline the considerations following identification of orf on AMI
- Zoonotic by contact
- Extensive/advanced disease highlights welfare issue on farm
- Likely to be associated with emaciated animal
- Report to APHA and trading standards if extensive and causing welfare issue
Outline considerations followig sudden death at slaughterhouse
- Anthrax
- May also be electrocution, clostridial disease
- May be zoonotic
- Report to APHA
- Blood test from ear
What test is used to identify anthrax?
Staining of blood sample with polychromemethylene blue (violet pink surrounded by pink halo indicates anthrax)
Outline the considerations following identification of ulcerations and degeneration of tissue in the mouth of cattle/sheep on AMI
- Potentially FMD
- Notify APHA
- Sheep lesions not as evident as in cattle
Outline the considerations following identification of ulcerations in pigs mouth/snout
- Could be FMD or vesicular disease
- Appear the same clinical
- Notify APHA
Outline the considerations following identification of neurological signs on AMI
- Scrapie/BSE potential, notify APHA
- Also trading standards as should not have been transported
- Potential for Listeria (zoonotic)
- Aujeszky’s disease (exotic to UK, notify APHA)
Describe the clinical signs of Listeria
- Abortion at end of pregnancy
- Paralysis
- Salivation
- Tongue out to side of mouth
Outline the considerations following identification of lesions in mouth, swollen tongue and haemorrhage under the skin on AMI
- Bluetongue potential
- Most signs are non-pathognomic so need to consider time of year ad place of origin
Outline the considerations following identification of Actinomyces on AMI
- Can lead to emaciation
- Welfare issue
- Potentially zoonotic
- Only head needs to be rejected
- No need to notify APHA and Trading standards
Outline the considerations following identification of emaciation on AMI
- Unfit for slaughter, rejection
- Potential referral to APHA and Trading Standards (welfare issue)
Outline the considerations following identification of a severely lame animal on AMI
- Kill in situe, cannot be moved to stunning box
- Emergency slaughter so AMI still required
- Contact APHA and Trading standards
Outline the consideration following identification of abnormal growths/malformations on AMI
- If able to stand/walk independently and no signs of generalised infection, refer to APHA after death of animal for investigation
- Slaughter permitted with partial rejection where no signs of systemic infection
- Where systemic infection indicated, entire carcass rejection
What is the purpose of the PMI?
- Supplement AMI
- Detect diseases, residues, contaminant
- Identification of other conditions rendering unfit for human consumption
- Animal welfare