Operational procedure: As required food sample collection
On this page
- 1.0 Purpose
- 2.0 Authorities
- 3.0 Reference documents
- 4.0 Definitions
- 5.0 Acronyms
- 6.0 Operational procedure
- 7.0 Appendix
1.0 Purpose
The purpose of this document is to provide guidance to Canadian Food Inspection Agency (CFIA) inspection staff on the procedures for as required sample collection under the Food Business Line (FBL).
This guidance is written with the assumption that inspection staff have been trained in the Standard Inspection Process (SIP) and the Digital Service Delivery Platform (DSDP).
This document is intended to be used in conjunction with Operational guideline: Food sample collection.
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
Common inspection references
- Standard Inspection Process (SIP)
- Standard Regulatory Response Process (SRRP)
- DSDP Standard Operating Procedures (SOPs) (accessible only on the Government of Canada network)
- DSDP Inspection Case Management Guidance (accessible only on the Government of Canada network – RDIMS 14671957)
- LSTS User Services User Guide (accessible only on the Government of Canada network – RDIMS 3495373)
Food inspection references
- Business Rules of Use for the IMS (accessible only on the Government of Canada network)
- CFIA Sampling Information (accessible only on the Government of Canada network)
- Food incident response process (FIRP)
- Food inspection guidance: permission issuance
- Food inspection guidance: sample collection (accessible only on the Government of Canada network)
- Food misrepresentation direction (accessible only on the Government of Canada network – RDIMS 13862494)
- Issues Management System User Manual (accessible only on the Government of Canada network – RDIMS 1599661)
- Operational guideline: food regulatory response guidelines
- Operational guideline: Food sample collection
- Operational procedure: Responding to food complaints (accessible only on the Government of Canada network - RDIMS 13899359)
- Operational procedure: Official food sample collection
- Operational procedure: Planned food sample collection
- Protocol for CFIA's Sharing of Information during Food Safety Investigations and Recalls
Commodity specific inspection references
DSDP sample collection specific references
4.0 Definitions
Definitions are located in the documents listed below:
- Safe Food for Canadians Regulations: Glossary of key terms
- My CFIA glossary of terms
- Canadian Food Inspection Agency – Health Canada Food Sampling and Testing Terminology
- Operational guideline: Food sample collection
5.0 Acronyms
Acronyms are spelled out the first time they are used in this document and are consolidated in the Food business line acronym list.
6.0 Operational procedure
This operational procedure provides inspection guidance specific to as required food sample collection and is to be used by CFIA inspection staff when there is a trigger for sample collection outside of the Food Sample Collection Plan (accessible only on the Government of Canada network) and sample collection activities are required in response to an event.
An inspector may collect an as required sample when suspected problems need to be investigated and/or verified. As required samples are normally unplanned and collected in response to an event (for example, a complaint, a failed monitoring sample or when a potential non-compliance is identified, refer to Table 1 for as required permission triggers).
This operational procedure applies to as required samples collected at all regulated parties (including SFCA license holders and non-license holders), at all levels of distribution (including retail, manufacture, import and storage) and at the harvest area.
6.1 Prepare for the inspection
Refer to SIP, Section 3, Step 1 and Operational guideline: Food sample collection, Section 6.1. In addition to the general guidance provided in these documents, the following guidance applies to as required sample collection.
Inspectors should consult with their supervisor, Regional Program Officer (RPO), Area Recall Coordinator (ARC) / Regional Recall Coordinator (RRC), Regional Coordinator (RC), the Office of Food Safety and Recall (OFSR) and Laboratory Coordination Division at any point in the as required sampling process if questions arise.
Inspectors must determine the scope of the as required sample collection by considering:
- the as required sample collection trigger (refer to Table 1 for examples)
- the techniques and types of sample analysis required (refer to Table 2. Specific sample collection techniques applied during sample collection and Appendix 6: Types of analyses for food samples in Operational guideline: Food sample collection)
- the commodity specific sampling methods required (refer to Table 3. Commodity specific sampling methods in Operational guideline: Food sample collection)
As required sample collection trigger: | When applied a sample collection activity is required to: |
---|---|
Incident Response (Issues Management System (IMS) and/or DSDP) | Aid in verification of a suspect or realized risk |
Domestic Permission (DSDP) | Support the issuance of a domestic permission |
Import Permission (DSDP) | Support the issuance of an import permission |
Export Permission (DSDP) | Support the issuance of an export permission |
Additional steps should be considered when preparing for an as required sample collection activity (refer to Table 2).
If sample collection includes: | Then: |
---|---|
A potential food safety incident | Consult with the Office of Food Safety Recall (OFSR) and refer to: |
Commodity specific sample | Refer to:
|
Urgent or investigative samples Uncertainty as to where to send sample for analysis A sampling plan quota that has been reached and additional samples are required |
Contact: Laboratory Coordination Services |
Taking a sample to verify:
|
Refer to: |
Taking a sample when non-compliance is suspected |
Refer to: |
Taking a sample that requires the lot be ordered not to move pending results | Refer to: |
6.2 Conduct the inspection
Refer to SIP, Section 4, Step 2 and Operational guideline: Food sample collection, Section 6.2. In addition to the general guidance provided in these documents, the following additional information may be required for as required sample collection.
6.2.1 Record information
Sample collection data is captured in the Laboratory Sample Tracking System (LSTS). Samples should also be tracked in DSDP and/or IMS depending on the trigger for the sample collection. If using both DSDP and IMS ensure the IMS file number is inputted into DSDP in the 'Additional Reference IDs' field and the DSDP case number is inputted into the IMS file. Refer to Table 3 for examples of when sample collection data may be recorded into each system.
Data System: | When used: | Additional resources: |
---|---|---|
LSTS (sample collection data) |
LSTS is the primary system for collecting data on sample information and resulting laboratory assessments for as required samples. | LSTS User Services User Guide (accessible only on the Government of Canada network – RDIMS 3495373) |
DSDP (sample tracking data) |
DSDP is used to capture time taken for sample collection, other than satisfactory sample results and follow-up unless the task is triggered by a complaint or the Food incident response process (FIRP). Note: Task time entries are recorded in DSDP for the time associated with sample collection only. The time taken to enter the samples into LSTS or shipping of the samples is not included in DSDP. |
DSDP Standard Operating Procedures (SOPs) (accessible only on the Government of Canada network) |
IMS (sample tracking data) |
IMS is used to track sample collection activities when the sample collection task is triggered by a complaint or food safety investigation. Note: Time spent on the food safety investigation and/or complaint follow-up, including, but not limited to the recall activities, effectiveness checks etc. should be tracked in IMS |
Business Rules of Use for the IMS (accessible only on the Government of Canada network) |
If a new DSDP case is created for an as required sample, one of the four triggers listed in Table 4 must be chosen and the appropriate task data must be entered.
If as required samples are collected as part of a PC inspection, commodity inspection, or sample collection activity, the inspector is not required to create a new case. The inspector can add a DSDP inspection task for the as required sample to the existing case, starting at Inspection task level 1. Refer to Table 4 for data entry details.
Trigger | Choose one of the following triggers as appropriate:
|
---|---|
Inspection task type | Sample Collection |
Inspection task level 1 | Food Sample Collection Plan |
Inspection task level 2 | Select the appropriate analysis type:
|
The first part of the sample collection task is now complete; the sample has been collected and sent to the lab for analysis. The second part of the sample collection task will be initiated once the sample results are received.
6.2.2 Determine if immediate control action is required
Review the sample results once received to determine next steps. If sample results indicate the need to control a potential risk, inspectors will follow the FIRP. Refer to SIP Section 4.5 for additional information.
Refer to Food inspection guidance: incident response for further guidance that may be applicable to sample results requiring further action.
6.2.3 Determine compliance
The inspector is required to review the results to determine compliance based on the reason for sampling. Refer to SIP Section 4.6.
Sample results reported as anything other than satisfactory require further action and must be documented in DSDP and/or in IMS.
If a sample is non-compliant, consult SIP, Section 4.7. A non-compliance record must be created in DSDP and/or the IMS file must be updated accordingly.
6.2.4 Categorize non-compliance
Non-compliant as required samples are categorized based on the sampling trigger (Table 1), the risk and the potential impact. Refer to the SIP, Section 4.7 for more information.
6.2.5 Record sample results in DSDP and/or IMS
Refer to Table 5 for further information on how the inspectors will record the sample results in DSDP and IMS.
Result | Action / Resources |
---|---|
Satisfactory | If a DSDP case was opened, satisfactory results should not be entered into DSDP and would not need to be communicated to the regulated party, unless the lot was ordered not to be moved pending results. If an IMS issue was opened, Satisfactory results should be entered into IMS. Refer to Issues Management System User Manual (accessible only on the Government of Canada network – RDIMS 1599661), as applicable, for additional information. |
Other than satisfactory |
If a DSDP case was opened, refer to Annex B: DSDP data entry – CFIA sampled – sample results other than satisfactory (accessible only on the Government of Canada network – RDIMS 14996797) beginning at step 6. If a DSDP case needs to be reactivated, refer to Annex B: DSDP data entry – CFIA sampled – sample results other than satisfactory (accessible only on the Government of Canada network – RDIMS 14996797). If a DSDP case was created, refer to SOP Creating an Inspection Request (accessible only on the Government of Canada network – RDIMS 9852034), for instructions on how to add a DSDP inspection task and SOP Manage Samples (accessible only on the Government of Canada network – RDIMS 9852138) for instructions on how to complete the information in the inspection task. If an IMS issue was opened, other than satisfactory results should be entered into IMS. Refer to Issues Management System User Manual (accessible only on the Government of Canada network – RDIMS 1599661), as applicable, for additional information. |
6.3 Communicate the results
Refer to SIP, Section 5, Step 3 and Operational guideline: Food sample collection, Section 6.3. In addition to the general guidance provided in these documents, refer to Table 6 for additional information on how to communicate the sample results for as required sample collection.
Reason for sample collection: | Details on results communication: | Additional Resources: |
---|---|---|
Food safety investigation / Complaint follow up | Inspectors performing the sampling activities should communicate results to the lead inspector / recall coordinator / OFSR and/or the regulated party as applicable. Laboratory results generated by the CFIA for either a complainant's sample that was turned over to the CFIA or for a sample taken by the CFIA in relation to the complaint investigation may be communicated to the complainant. |
Protocol for CFIA's Sharing of Information during Food Safety Investigations and Recalls |
To verify compliance at a regulated party |
If the lot is ordered not to be moved, the inspector will communicate the results and/or the next steps to the regulated party, for example if product may be released or further action is required. When non-compliant domestic samples are identified, Area/Regional Operations may communicate the results to the appropriate Provincial authorities for follow-up. |
6.4 Conduct the follow-up inspection
Refer to SIP Section 6, Step 4. In addition to the general guidance provided in these documents, the following guidance applies to sample collection.
For general inquiries related to this Operational Procedure, follow established communication channels including the submission of an electronic Request for Action Form (e-RAF) (accessible only on the Government of Canada network).
7.0 Appendix
Annex B: DSDP data entry – CFIA sampled – sample results other than satisfactory
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