Operational procedure: Visual examination of container integrity
On this page
- 1.0 Purpose
- 2.0 Authorities
- 3.0 Reference documents
- 4.0 Definitions
- 5.0 Acronyms
- 6.0 Operational procedure
1.0 Purpose
The purpose of this document is to provide Canadian Food Inspection Agency (CFIA) inspection staff with the procedure to verify that packaged food in Canada is safe, wholesome and meets the requirements of the Safe Food for Canadians Act and Regulations and the Food and Drugs Act and Regulations.
This document is intended to be used in conjunction with the Standard Inspection Procedures and the Operational Guideline on General Principles of Sampling.
The guidance outlined below may be used to aid in the assessment of a Preventive Control Plan (PCP) related sub-element, or as part of a food safety investigation or follow-up to a complaint.
2.0 Authorities
- Safe Food for Canadians Act (SFCA)
- Safe Food for Canadians Regulations (SFCR)
- Food and Drugs Act (FDA)
- Food and Drug Regulations (FDR)
The inspection powers, control actions and enforcement actions authorized by the above legislation are identified and explained in the Operational guideline – Food regulatory response guidelines.
3.0 Reference documents
- Standard inspection procedure (SIP)
- Operational procedure – Meat Compliance verification system (CVS)
- Standard Regulatory Response Process
- Operational guidance – Food regulatory response guidelines
- Food Incident Response Process
- Operational guideline – General principles of sampling
- Operational procedure – Procedure for seizure and detention, authorizing movement and disposition
- Industry guidance – Visual Examination of Commercially Sterile Low-Acid and Acidified Low-Acid Foods Packed in Hermetically Sealed Containers
- Industry guidance – Metal Can Defects – Identification and Classification
- CFIA Sampling Information (internal access only)
- Inspection Worksheet: Visual Inspection of Hermetically Sealed Containers (internal access only) – RDIMS 11442331
4.0 Definitions
Unless specified below, definitions are located in either the:
- Safe Food for Canadians Regulations: Glossary of key terms
- Integrated Agency Inspection Model (iAIM) – Glossary of terms (Annex F)
- My CFIA Glossary of terms
For the purpose of this document the following definitions apply:
- Low-acid food
- means a food, other than an alcoholic beverage, where any component of the food has a pH greater than 4.6 and a water activity greater than 0.85
- Acidified low-acid food
- is a food that has been treated by pickling or fermentation so as to attain an equilibrium pH of 4.6 or lower after heat processing (for example pickles)
- Hermetically sealed
- means a container designed and intended to be secure against the entry of microorganisms, including spores
- Commercially sterile
- means the condition obtained in a food that has been processed by the application of heat, alone or in combination with other treatments, to render the food free from viable forms of microorganisms, including spores, capable of growing in the food at temperatures at which the food is designed normally to be held during distribution and storage.
5.0 Acronyms
Acronyms are spelled out the first time they are used in this document and are consolidated in the Food business line acronyms list.
6.0 Operational procedure
6.1 Procedure for low-acid food product or acidified low-acid food product in a metal can
6.1.1 Inspect the selected container and complete the appropriate worksheets
Inspect the containers according to the Visual Examination of Commercially Sterile Low-Acid and Acidified Low-Acid Foods Packed in Hermetically Sealed Containers.
Use the same terminology and classification of defects as described in the Metal Can Defects – Identification and Classification.
The worksheet Visual Inspection of Hermetically Sealed Containers (internal access only – RDIMS 11442331) is available as a tool for recording observations. Enter inspection findings into (data capture system to be determined).
6.1.2 Follow up
Unsatisfactory Inspection Results: When the results of the visual examination are unsatisfactory (that is one or more serious defects are found):
- Detain the inspection lot and other suspect lots (if any). Use Operational procedure-Procedure for seizure and detention, authorizing movement and disposition.
- Determine if the lot(s) have been distributed and if so, follow the guidance in the Food incident response process and follow appropriate communication lines.
- Determine the cause and the extent of the issue (for example other lots produced on the same malfunctioning line, other lots produced with the same defective containers, other companies using the same defective containers).
- Refer to the CFIA Sampling Information (internal access only) for guidance in selecting an appropriate number of cans as per the directed sampling plan of the commodity (for example processed products) and send to the laboratory for commercial sterility and container integrity analysis. Notes: The laboratory analysis is the official confirmation of the container integrity verification.
If the Job Assessment on the Laboratory Report of Analysis is:
- Satisfactory: release the lot
- Investigative: select another appropriate set of samples and send them to the lab for analysis
- Unsatisfactory: follow the procedures in Visual Examination of Commercially Sterile Low-Acid and Acidified Low-Acid Foods Packed in Hermetically Sealed Containers (for example, culling procedures or disposition of the lot) and immediately notify the Regional Recall Coordinator if the product has been distributed
- If product is in distribution, document the findings in the Issues Management System (IMS) as per business rules.
- Follow the Standard Inspection Procedure (SIP) or CVS to verify that corrective actions implemented by licensed operators are effective to ensure safety of products received.
6.2 Inspection procedure for containers other than metal can for low-acid food product or acidified low-acid food product
Inspection protocols for other package types are currently under development.
For general inquiries related to this Operational Guidance Document, please follow established communication channels, including submitting an electronic Request for Action Form (e-RAF).
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