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The generic model was developed using the CFIA’s Food Safety Enhancement Program (FSEP)
approach and tools. It is a practical example for the operator of a storage facility to follow in designing
their own facility specific HACCP plan. The operator must review all potential health and safety hazards
in their operation and focus on controlling the points that are critical to food safety.
The committee wishes to emphasize that the model described here is a GENERIC MODEL. It does not
cover all storages, nor does it list all possible associated hazards. This generic model is a template that
can be adapted to most storage operations. Detailed information can be found in the FSEP Manual to aid
in the completion of the required forms.The process flow diagram in this generic model represents the
basic process steps from receipt of the incoming products through to shipping and distribution.
The HACCP team at each establishment is responsible for identifying and controlling all hazards
specific to its operation and for determining how each hazard is controlled. In order to identify all
possible hazards, the HACCP team should consult the Reference Database for Hazard Identification
developed by CFIA, along with the most current FSEP Manual, reference texts and scientific publications.
A review of the manufacturer’s processes and procedures should then be conducted to determine
whether each of the hazards identified in this generic model actually exist in the facility and to determine
how each of those hazards is controlled at each step in the process. Where products, procedures or
processes differ from those in the generic model, the HACCP team should determine whether process
steps should be added or removed. In addition, a hazard analysis should be conducted to determine
whether any hazards associated with those steps should be added or removed and to determine where
each of the additional hazards are controlled at the facility. As an example:
Freezing for Trichina control – While this generic model includes a step for the freezing of product
to control trichina if the facility does not conduct this process, this step would not be included in
the process flow. The step and the associated hazards would not appear on the hazard
identification and decision tree form and as a result, a CCP would not be identified.
This generic model indicates, as an example, the use of Method 3 from Annex B, Chapter 4 of the
Meat Hygiene Manual of Procedures. If the facility uses another method from Annex B, the
HACCP team must include the appropriate method(s) of Trichina control on Form 10. Each
method has its own set of regulated standards that must be met based on thickness, spacers,
temperatures etc.
Tempering for reinspection of meat products in this generic model is conducted in a room that is 4
°C or less. If tempering is conducted in a warmer room or in water, the HACCP Team must,
conduct a hazard analysis, determine whether any hazards associated with tempering must be
added or removed and determine how each of the hazards are controlled at this facility.
As a result of discussions during the development of this generic model, the following decisions and
assumptions were made:
It is the responsibility of the storage facility to ensure products received from clients are in
acceptable condition (e.g. acceptable and/or regulated temperature) and are maintained in that
condition.
It is the responsibility of the processing industry to ensure that the food sent to the storage has
been produced under conditions to prevent, eliminate or reduce contamination with pathogenic
bacteria. Storing and freezing operations do not eliminate pathogenic bacteria.
The receiving, storage, reinspection, and Trichina control of frozen and fresh pork domestic and
import loads, as well as other refrigerated products and dry goods are included in this generic
model.
Since it is impossible for the storage to maintain a current list of all products stored in the facility,
it is acceptable to reference a computerized database
The cold storage in this generic model receives both fresh and frozen pork. As required by the
Meat Hygiene Manual of Procedures (MOP) Chapter 4 Annex B, all pork must be fully frozen by
the operator prior to the start of the monitoring procedures to ensure the destruction of Trichina.
For freezing methods used to ensure the destruction of viable Trichinella in striated pork muscle
or meat product containing striated pork muscle, the operator is responsible for keeping current
and accurate records which document all parameters required for process control (e.g. lot
identification, time/temperature records), the critical limits which must be respected as well as the
actual measurements confirming that the critical limits were met and, when a process deviation
has occurred, the corrective action taken. Records shall be available to the inspector upon
request.
Lighting and other regulatory requirements for the re-inspection room must be addressed in the
Premises Prerequisite Program of the facility.
Operators should give consideration to the separation of incompatible goods to avoid issues of
cross-contamination and allergens.
As the use of cold storage facilities as distribution centres for food increases, the ability of the storage
facility to rapidly locate and identify product as an extension to the customer’s Recall procedures
becomes increasingly important, and must be given due consideration in the storage’s Recall Pre-
requisite Program.
For additional information concerning the control measures required to address the hazards associated
with the use of controlled freezing for the destruction of parasites such as Trichinella spiralis in pork, as
included in this Generic Model, refer to the Meat Hygiene Manual of Procedures, Chapter 4, Appendix B.
The generic or common name of the product family or process covered by the HACCP plan
shall be documented in form 1 or equivalent.
1. Product name(s) Meat and Non-Meat products
(See Computer Data Base for a complete list of
meat and non-meat products stored at the
establishment.)
2. Important product characteristics (aw, pH, Not applicable
preservatives, etc) It is the customers’ responsibility to conduct the
hazard analysis associated with their product
characteristics.
All ingredients, including composition of formulated ingredients (with reference to other documents if
needed), additives, processing aids and incoming materials that come in contact with the product or are
used in preparing the product shall be described in form 2 or equivalent, to the extent needed to conduct
the hazard analysis.
Water
BCP
Step 1
Receiving
BCP
Step 3-
Anti-parasite treatment for
Step 2-
pork
Tempering/
BCP
Re-inspection
BCP CCP 1B
Step 4-Storage
Cooler/Freezer
BCP
Step 5-
Shipping/Distribution
BCP
Plant specific
and
Note: This form is to be specific for each establishment. The plant schematic provides a basis for
evaluating potential areas of cross-contamination.
Plant schematic must be clear, accurate and sufficiently detailed. Plant schematic must at least include:
The HACCP team must verify the accuracy and completeness of the plant schematic by on-site checking.
The overall evaluation of potential areas of cross-contamination at the establishment should include any
other plant schematic from other HACCP plan(s).
Hazard Identification and Decision Tree - CCP Determination and other Control Measures (PP, PC) - FSEP forms 5, 6, 7, 8 and 9 combined into one form
COLD STORAGE / FREEZER FACILITY
Chemical
Potential contamination or cross Prerequisite programs:
contamination with chemicals through Transportation, Purchasing/
damaged / breached primary packaging Receiving/Shipping and Storage
(e.g. from fork lift accidents, improper B 2.2.2
stacking procedures).
YES General Food Hygiene Program
D 2.1.1
Physical
Potential contamination or cross Prerequisite programs:
contamination with hazardous extraneous Transportation, Purchasing/
material through damaged / breached Receiving/Shipping and Storage
primary packaging (e.g. from fork lift B 2.2.2
accidents, improper stacking procedures).
YES
Chemical
Potential contamination or cross Prerequisite programs:
contamination with chemicals through Transportation, Purchasing/
damaged / breached primary packaging Receiving/Shipping and Storage
(e.g. from fork lift accidents, improper B 2.1.2, B 2.2.2
stacking procedures).
YES
Physical
Potential contamination or cross Prerequisite programs:
contamination with hazardous extraneous Transportation, Purchasing/
material through damaged / breached Receiving/Shipping and Storage
primary packaging (e.g. from fork lift B 2.1.2, B 2.2.2
accidents, improper stacking procedures).
YES General Food Hygiene Program
D 2.1.1
Process CCP Hazard Critical Limits Monitoring Procedures Deviation Procedures Verification Procedures HACCP
Steps /Hazard Description Records
number
Process CCP Hazard Critical Limits Monitoring Procedures Deviation Procedures Verification Procedures HACCP
Steps /Hazard Description Records
number
Step 3- CCP-1B Biological Product placed in The product to be treated will If the temperature is interrupted (above -18°C) [Specify frequency], the HACCP Team Freezing
Anti-parasite Potential freezer in a frozen be placed in the Trichinella before the 106 hours has been met the Leader performs a record review and an Charts
treatment for survival of state at room. A thermocouple is freezing chart does not get signed and the onsite observation of the person
pork Trichinella -18 °C for 106 hours placed in the centre of the process starts over again once the inspector performing the monitoring task to Freezing
spiralis due to (uninterrupted) thickest piece of meat and in unlocks the room. If the core temperature has determine that: Log Book
inadequate Meat Hygiene MOP the warmest location of the lost -18C, then the product returns to the blast • The control measure within the
time / Chapter 4, freezer. Before the treatment cell to obtain -18C again. CCP has been operating as Corrective
temperature Annex B, Method 3. starts, the CFIA inspector will intended. Action
applications seal the doors to the room with The designated employee conducts/performs • Monitoring and deviation Report
a lock. the following procedures, using the Corrective procedures are conducted
Action Report according to the written program. CCP-1B
The internal temperature of 1. Records a description of the deviation • The CCP is effective in maintaining Verification
product will be monitored and and its cause. control of the hazard and that there Record
continuously recorded through 2. Take actions to control affected product. is no identified loss of control or
the “mis-probe” website. The 3. Implements corrective actions to restore trends in monitoring that may
designated employee monitors control of the CCP. The complete indicate development towards a
the time/temperature through treatment must be restarted again loss of control at the CCP
the “mis-probes” portal every (Product placed in freezer in a frozen Record Review
[specify frequency]. state at -18 °C for 106 hours For every Lot of product undergoing
(uninterrupted)) parasitic treatment, the HACCP Team
When the treatment is 4. Verifies the effectiveness of the Leader performs the following
successfully completed (106 corrective actions taken o Reviews all records documenting the
hours at -18°C), the 5. Evaluates the need to implement monitoring activities (Freezing Charts
designated employee prints additional measures to prevent and Freezing Log Book) generated since
the Freezing Chart and signs reoccurrence of the deviation. the last verification;
it. 6. Verifies the effectiveness of preventative o Reviews all records documenting the
measures if taken. actions taken in response to a
The designated employee deviation activities (Corrective Action
records the lot number, The designated employee documents all Report) generated since the last
product description, number of information and results of actions or verification.
boxes, date and time into the procedures followed on the Corrective Action On-site Review
freezer, date and time out of Report. The designated employee initials and The HACCP Team Leader performs the
the freezer on the Freezing dates each entry and records the exact time following;
Log Book. each entry is made. o Observes the monitor perfoming the
monitoring activities and interviews
The designated employee employee(s) responsible for monitoring
notifies the CFIA inspector. and deviation
The Freezing Chart and the When the results of the verification
Freezing Log Book will be demonstrate that the monitoring or
presented to the CFIA deviation activities are not conducted
inspector for release of the according to the written program, the
product. CCP is not effective to maintain control
of the hazard or there is a trend towards
a loss of control, the HACCP Team
Leader shall follow the Deviation
Procedures as stated in the CCP.