Revised: 2009-12-21
Recycled food products (RFPs) are materials that remain after, or are produced during, the processing, manufacture, preparation or sale of human food. RFPs may, under certain conditions, be suitable for use as livestock feeds. This section sets out the regulatory requirements for RFPs intended as livestock feeds in Canada. The information contained herein is pertinent to food processing plants, feed mills, RFP manufacturers, distributors, and all other persons involved with the manufacture, importation, sale or distribution of RFPs in Canada.
Although these products are generated as by-products of human food production, it is important to stress that the livestock feed chain is not a means to dispose of degraded or contaminated foodstuffs, and that the product must have a nutritional value to be considered a feed.
RFPs that are currently approved as single ingredients for use in livestock feed are listed in Schedule IV of the Feeds Regulations. Examples include Bakery waste dehydrated (4.6.1), Cereals breakfast process residue (4.6.7), and Wheat distillers grains dehydrated (5.5.21). For a complete and up-to-date listing, please contact the Animal Feed Division of the Canadian Food Inspection Agency (CFIA).
If an RFP meets an existing definition as listed in Schedule IV, Part 1, namely, a substance that has been assessed or evaluated as acceptable for use in feed, and meets the standards, packaging and labelling requirements set out in the Feeds Regulations, it may be manufactured, sold, imported or distributed as a single ingredient feed without registration. If an RFP meets an ingredient definition as set forth under Schedule IV, Part 2, OR if it contains two or more single ingredient feeds listed in Schedule IV or V, it must be registered with the Animal Feed Division. If an RFP does not meet any approved feed definitions or requires registration, it is not to be manufactured, sold, imported or distributed as a feed without prior approval of the Animal Feed Division. Please refer to Section 1.1, "Application for Feed Registration and Ingredient Approval".
RFPs should be handled, transported and stored in a sanitary manner in order to prevent contamination and the growth of pathogenic organisms, or the production of harmful toxins (e.g., mycotoxins). The risk of contamination by microbial or chemical impurities must be minimized for all livestock feeds.
Feed manufacturers and livestock producers are responsible for ensuring that suppliers apply quality control procedures, and that appropriate hygienic practices are followed in the collection, handling, transportation, and storage of the RFP.
Due to the risk of zoonotic and exotic diseases, meat products, meat by-products and products suspected to contain meat are not permitted in RFPs intended for livestock feed unless they:
If an RFP contains meat or is sourced from a facility where there is meat present (including sandwich meats, filler, beef patties, plate waste, restaurant preparation waste, etc.), including facilities where products are sorted and separated from products containing meat, it is prohibited from being sold, manufactured, imported or distributed as feed, without prior approval of the Animal Feed Division.
NOTE: RFPs that are exempt from the Feeds Act and Regulations are still subject to the Health of Animals Regulations. These RFPs must meet conditions a) and b) above, and RFPs that are to be fed to swine or poultry must also comply with condition c).
The following identifies the registration and approval requirements for RFP ingredients per the Feeds Act and Regulations. Please note that additional information beyond what is listed in this section may be requested, on a case-by-case basis, after review of the submitted information. In order to facilitate the evaluation process, it is recommended that applicants contact the Animal Feed Division prior to submitting an application for ingredient approval or registration.
A) Registration and Ingredient Approval Information
Information on registration and ingredient approval requirements can be found in Chapter 1.
Please see the "Registration Checklist for Recycled Food Products (RFPs) to be Used as Livestock Feed Sources" below, which summarizes the basic requirements for all RFP submissions.
B) Composition and Manufacturing Conditions
A detailed description of the manufacturing process for the submitted RFP
must be provided, including the source and description of all individual ingredients that enter into the manufacture of the
RFP. This information includes, but is not limited to:
If, following approval/registration, there are changes in the composition of the RFP (e.g., a new ingredient or source), the manufacturing process, or other conditions, the Animal Feed Division must be notified.
C) Quality Control Procedures
Since RFPs are exposed to multiple handling, storage, and transportation
conditions, temperature variations, etc., a detailed description of the quality control
procedures is required. This includes, but is not limited to:
D) Safety Data
Data demonstrating the safety of the RFP must be provided, including the
following information:
Identification of potential chemical contaminants and sources of contamination
It may be necessary to submit additional safety data for any contaminants present in the RFP. Based on the data submitted, a scientific rationale may be required to demonstrate that the levels present in complete feed do not result in adverse effects on the intended species of livestock or to human health. The toxicity data may be obtained from complete scientific articles in refereed journals, information from toxicity databases, or unpublished toxicity studies with all the data provided. Abstracts and testimonials are not acceptable.
Microbial Contamination, Shelf-life, and Stability
These analyses must be provided with the application for approval or registration. In some cases, analyses may be omitted when justified by a scientific rationale, supported by peer-reviewed literature.
It is recommended that applicants contact the Animal Feed Division well in advance of submitting an application for approval or registration to determine the types of analyses that may be required.
E) Efficacy Data
RFPs must have a nutritional purpose to be acceptable as livestock feeds.
Product labels and supporting information must indicate the target species, the typical and maximum feeding or usage rate,
and nutritional guarantees. Supporting Certificates of Analysis (signed originals) for three (3) production lots of the
finished RFP are required to characterize the nutrition of the product and
to support the proposed label guarantees. The certificates must include analysis of percent moisture content. The
certificates must include analysis of added or inherent sources of nutrients (e.g. protein,
fat, fibre, sugars, vitamins, minerals) to determine if these nutrients are present at significant levels. Note that
scientific studies may be required to support the usefulness of the ingredient.
Certificates may be required for nutritional analysis at the end of the proposed shelf life period, depending upon the type of product being manufactured. In these cases the laboratory should analyze the same lots over the time period specified (i.e. sample from the production lot and store the sample; and then resample same production lot sample at the end of the time period). The product samples should be stored under conditions representative of the storage conditions used in the field.
F) Facility Inspections
Before approval or registration, an inspection of the facilities that manufacture, collect, or process RFPs destined for livestock feed may be conducted. These facilities, like other
feed producing facilities, will be subject to periodic monitoring inspections and random sampling by CFIA inspection staff to verify that the feeds comply with regulatory
requirements.
Table 1. Minimum microbial indicators and physical criteria required for assessing the risk of microbial pathogens and contaminants of concern in recognized categories of recycled food products prior to feeding to livestock. Recommended storage conditions, and approximate shelf life are provided.
| Classification of Recycled Food Product1 |
Microbial Indicators/ Physical Criteria |
Storage Conditions | Approximate Shelf Life2 |
|---|---|---|---|
| Dry foods | Yeasts Moulds ACC3 Salmonella spp. E. coli Mycotoxins4 Water activity (aw) |
dry, protected from pests | 30-60 days |
| Milk and dairy based foods | Yeasts Moulds ACC3 LAB5 Coliforms Salmonella E. coli L. monocytogenes6 Salmonella spp. pH |
protected from pests | 3-7 days |
| Wet vegetables and vegetable residues | Yeasts Moulds ACC3 LAB5 Enterobacteriaceae Salmonella E. coli L. monocytogenes6 Mycotoxins4 pH |
protected from pests | 3-7 days |
| Wet fruit and fruit residues | Yeasts Moulds ACC3 LAB5 Enterobacteriaceae Salmonella E. coli L. monocytogenes6 Mycotoxins4 pH |
protected from pests | 3-7 days |
| Dried fruit and fruit residues | Yeasts Moulds ACC3 Enterobacteriaceae Salmonella spp. E. coli Mycotoxins4 Water activity (aw) |
dry, protected from pests | 30-60 days |
| Nuts | Moulds ACC3 Coliforms Salmonella spp. E. coli Mycotoxins4 Water activity (aw) |
dry, protected from pests | 60 days |
1 This is not intended to be a comprehensive list, i.e. there may be other types of RFPs that are not included.
2 The approximate shelf life values are estimates and should be substantiated by actual testing and inspection of the product. Shelf life will be dependant upon climate, moisture, hygienic and storage conditions. Recycled food products displaying obvious signs of decomposition should not be fed to animals even if the proposed shelf life has not been exceeded.
3 ACC = aerobic colony count
4 Mycotoxin fact sheet is available at www.inspection.gc.ca/english/anima/feebet/pol/mycoe.shtml.
5 LAB = lactic acid bacteria
6 Storage conditions are unlikely to include refrigeration temperatures and ruminants are more susceptible than pigs to L. monocytogenes infection, so it may be advisable to restrict this allowable limit to pigs, with a limit of 0 colony-forming unit per gram (CFU/g) for ruminants.
Administrative Registration Requirements
Completed application package per Chapter 1
Proposed Label
Brand name (optional)
Product name reflecting purpose of the product and the intended species
Guaranteed analysis
Directions for use to permit safe and effective use of feed (including feeding rate)
Caution and/or warning statements (if applicable)
Name
and address of registrant
Net
amount (metric measure)
Date
of Manufacture
Expiration date
Registration number (to be added)
Product Composition
List of all food ingredients/products that may be mixed into each product
Source of each ingredient, including the name and contact information of each supplier
The product formulation (note that a range may be used)
List of products added during the manufacture, processing and storage of the RFP
Manufacturing Conditions
Detailed explanation of the manufacturing process used to generate the final product
Description of the storage of the products
Quality Control Procedures
Records (from each supplier) detailing the origin of the food product ingredients and the reasons for rejection
Written procedures used to screen ingredients for contaminants
Records demonstrating that written procedures were followed
Safety Review
Identification of potential chemical contaminants and sources of contamination
Signed Certificates of Analysis for relevant contaminants for three (3) different lots of the RFP ingredient
Proposed shelf life
Certificates of Analysis for a minimum three (3) different lots of finished product for the specified indicators
Matching Certificates of Analysis of the same three lots from the end of the proposed shelf life. Note: this requirement is
dependent upon on the proposed shelf life and the type of product being manufactured
Efficacy Data
Supporting Certificates of Analysis (signed originals) for three (3) production lots for the nutrient content of the
finished RFP, including added nutrients and moisture.
Certificates may be required for the same lots at the end of the proposed shelf life period depending upon
the type or product being manufactured.
Facility Inspections
The RFP supplier/manufacturer may be subject to a pre-approval plant
inspection to verify the information submitted.
The RFP supplier/manufacturer may be subject to monitoring inspections to
confirm continued compliance.
Note: Further information may be required after a review of the preliminary submission.