Unlabeled or Exclusive Products - U.S. Produced | Supplier Imported
Sites producing unlabeled or exclusive products must obtain and maintain GFSI-recognized certification. Failure to maintain annual certification may result in loss of business and deactivation of your vendor number. GFSI-recognized certification is required for all sites that manufacture or process unlabeled or exclusive product that will be sold at Walmart and/or Sam’s Club, regardless of ownership. It is the responsibility of the supplier to ensure all sites manufacturing or processing unlabeled or exclusive products maintain compliance with our audit requirements – Walmart does not schedule audits for suppliers or sites. Suppliers will be required to disclose their supply chain to ensure compliance with these requirements. Any changes to supply chain sites shall be communicated to your Food Safety manager. New sites must have approval prior to use.
Please be aware that if you supply frozen berries or frozen berry blends, the entire supply chain from farm to final facility is required to obtain GFSI-recognized certification, be disclosed, and any changes in sites must be approved before use.
For more information about the GFSI-recognized certification process and to view a full list of recognized schemes, we recommend visiting the official GFSI website.
Walmart requires suppliers of specific commodities to go above and beyond complying with audit and regulatory requirements to ensure the safety of their products. In addition to GFSI-recognized certification, these suppliers must also comply with all commodity specific requirements prior to providing their products to our stores, clubs, or websites.
Listeria monocytogenes is a recognized human pathogen commonly associated with ready-to-eat food items, including deli meats. In our ongoing commitment to the health and safety of our customers and members, Walmart, Inc. mandates that all suppliers of bulk deli meats intended to be sliced in our stores/clubs and pre-packaged sliced deli meats adhere to the following requirements.
- Every SKU of bulk deli meat intended to be sliced within our stores/clubs must include an antimicrobial agent (as defined in 9 CFR 430.1) that will not allow Listeria monocytogenes to increase more than 1-log during the intended shelf-life and storage of the product. Effectiveness of the formulation must be verified through a scientifically credible challenge study.
- Every SKU of pre-packaged sliced deli meat must include an antimicrobial agent (as defined in 9 CFR 430.1) that will not allow Listeria monocytogenes to increase more than 1-log during the intended shelf-life and storage of the product. Effectiveness of the formulation must be verified through a scientifically credible challenge study.
- We recommend that all deli product labels be as clean as possible. Therefore, any antimicrobial agents used shall be consumer accepted, food-grade preservatives that do not negatively impact product quality or taste. Additionally, whenever possible, these antimicrobial agents should be of natural origin.
- Suppliers must have a comprehensive, multifaceted Listeria control program including strict sanitation, environmental monitoring, and finished product testing. These programs are required for all sites manufacturing or processing product that will be sold at Walmart and/or Sam's Club, regardless of ownership. Corresponding documents and records relating to deli products produced under the scope of this requirement must be made available upon request.
Suppliers must submit challenge studies for each item number or formulation to undergo our review before receiving approval to supply the product to our stores and/or clubs.
Ongoing monitoring & verification of compliance with these requirements will occur every 3 years, at a minimum. Suppliers should notify Walmart, Inc. Supplier Food Safety as soon as possible when there are changes to:
- Product formulation,
- Raw material suppliers,
- Ingredient and/or packaging material specifications,
- Manufacturing site or equipment (e.g., line changes that impact product flow, process changes that alter process control, manufacturing zoning changes, installation of new equipment).
In these instances, a new study may be required or appropriate scientific justification to support use of an existing study must be provided.
Suppliers providing fresh shell eggs to Walmart and/or Sam’s Club are required to comply with the Best-in-Class (BIC) Fresh Shell Egg requirement guide. Please contact your Walmart or Sam’s Club merchant for a copy of this guide to ensure your compliance with all food safety requirements.
Please refer to the table below for the most up-to-date list of accepted, non-antibiotic feed additives approved for use by Walmart.
MANUFACTURER PRODUCT RATE OF INCLUSION
| Cage/Cage-Free (lb/Ton) |
Outdoor Birds Organic/Pastured (lb/Ton) |
||
| Alltech, Inc. | Actigen | 0.4 - 1.6 | 0.4 - 1.6 |
| Arm & Hammer | Celmanax Dry NC (product with carrier) |
2 | 2 (only for non-organic pastured birds) |
| Celmanax SCP NC (pure product without any carrier and color) |
0.2 | 0.2 | |
| Diamond V | XPC | 1.5 | 2.5 |
| QTI/Calpis | Calsporin 1.0B | 0.5 | 1.0 |
| Calsporin | 0.25 | 0.5 | |
| Calsporin Organic | 0.5 | 1.0 | |
| Calsporin Organic 2.0 | 0.25 | 0.5 | |
| IMW50 | 1.0 | 2.0 | |
| Backpak | 1.0 | 1.5 | |
Frozen berries and frozen berry blends have been increasingly associated with foodborne disease outbreaks over the past couple of years. The most common pathogens identified have been norovirus, hepatitis A, and Shigella sonnei. Due to heightened risk and consumer awareness, we require all frozen berry and frozen berry blend suppliers to comply with the following requirements.
- Suppliers should ensure all operations have adequate food safety programs in place including handwashing programs, access to restroom facilities, routine food safety training, and actionable employee illness policies. These programs should be implemented at all operations that handle the berries from harvest locations to final packaging facilities, regardless of ownership.
- Many of the berries associated in outbreaks have been sourced from countries which had previously been implicated in viral outbreaks. Suppliers are to avoid sourcing berries from countries and geographical regions known to have endemic levels of hepatitis A or other pathogens of concern.
- Suppliers are encouraged to consider the immunization of field workers, regardless of the countries used to source berries.
These requirements are applicable to suppliers who provide fresh or frozen products containing raw ground beef or raw ground bison. It should be noted that these requirements are applicable to product sold raw to our customers/members as well as product that is supplied raw to our stores and clubs which will be cooked prior to being provided to our customers/ members.
Based on thorough consultation and consensus with numerous stakeholders from industry, academia, regulatory, and consumer groups, we require all suppliers that provide products containing raw ground beef or raw ground bison implement process control standards to protect against human pathogens such as Escherichia coli O157:H7 and Salmonella enterica serotype Newport. Suppliers of these products must comply with the following requirements.
- Suppliers must ensure the raw materials and/or finished product is tested for E. coli O157:H7 using approved testing methods and an N-60 sampling plan. If suppliers require this testing of their raw materials and are not conducting the testing within their facility, they are required to obtain a COA from their suppliers confirming this testing has been conducted and that all results were negative.
- Grind facilities that obtain trim solely from outside sources (not owned or controlled by their company) must implement a regulatory approved intervention or a combination of interventions within their grind facility that will consistently produce, at a minimum, a 2-log reduction of the pertinent microorganisms (enteric pathogens) on raw trim used for grinding. The intervention or combination of interventions must be scientifically validated at all grind operations regardless of ownership.
- Grind facilities that obtain trim from vertical sources (facilities owned or controlled by their company) must implement a regulatory approved intervention or a combination of interventions that will consistently produce, at a minimum, a 5-log reduction of pertinent microorganisms (enteric pathogens) within their slaughterhouse and/or grind operations. The intervention or combination of interventions must be scientifically validated at all operations. In addition, the vertical slaughter facilities providing raw trim used for grinding must also achieve and maintain GFSI-recognized certification annually.
Please be aware that suppliers will be required to submit scientific validations of their interventions for review and approval prior to being allowed to provide the product to our stores and clubs. It should also be noted that the microorganisms used for the validation must be indicative of enteric pathogens and APC counts will not be accepted. Product testing programs may also be requested for review at any time.
These requirements are applicable to suppliers who provide the fresh or frozen raw whole bird chicken, raw chicken parts, and raw ground turkey products. It should be noted that these requirements are applicable to product sold raw to our customers/members as well as product that is supplied raw to our stores and clubs which will be cooked prior to being provided to our customers/members, such as rotisserie chickens.
Poultry products have been involved in multiple high-profile recalls and outbreaks over the past decade. In light of these incidents, we require all poultry suppliers that provide the poultry products outlined above to meet our poultry safety initiative. Suppliers of these products must comply with the following requirements.
- To reduce the vertical transmission of Salmonella to broiler flocks, all poultry suppliers are expected to source from primary breeders who participate in USDA’s National Poultry Improvement Plan (NPIP) for Breeding Poultry (9 CFR 145.83). Countries outside of the U.S. that do not source from breeders participating in the NPIP program should source from breeders who comply with equivalent requirements.
- Salmonella data, obtained via the current NPIP programs, or equivalent, must be reviewed by your company on a regular basis to measure the effectiveness of preventive and corrective actions that occur when Salmonella is detected and to reduce the likelihood of re-occurrences.
- When Salmonella serotypes known to be associated with human illness are detected in a housing complex, suppliers must use autogenous and/or commercial Salmonella bacterins for vaccination of broiler-breeder (parental) flocks against the serotypes found. Moreover, to further control horizontal transmission at the broiler farm level, we expect all of our suppliers to strictly adhere to disease prevention best practices associated with biosecurity and vector control.
- Poultry suppliers must implement a regulatory approved intervention or a combination of interventions between pre-scald to post-chill that will consistently produce, at a minimum, a cumulative 4-log reduction of Salmonella. The intervention(s) and their corresponding reductions must be scientifically validated. Each facility processing whole chickens provided to our stores/clubs, whole chickens that are further processed into chicken parts that are provided to our stores/clubs, and whole turkeys that are further processed into ground turkey that is provided to our stores/clubs are required to comply with this requirement, regardless of ownership.
- Poultry suppliers providing raw chicken parts must implement a regulatory approved intervention or a combination of interventions post-chill, after cut-up of whole chickens (past the current whole bird carcass rinse sampling point), and prior to packaging. The intervention(s) must consistently produce a reduction of Salmonella on all chicken parts. The intervention(s) and their corresponding reductions must be scientifically validated. Each facility providing chicken parts is required to comply, regardless of ownership.
- Poultry suppliers providing raw ground turkey must implement a regulatory approved intervention or a combination of interventions post-chill, after cut-up of whole turkeys (past the current whole bird carcass rinse sampling point), and prior to packaging. The intervention(s) must consistently produce, at a minimum, a 1-log reduction of Salmonella on all ground turkey supplied to our stores and clubs. The intervention(s) and their corresponding reductions must be scientifically validated. Each facility providing ground turkey is required to comply, regardless of ownership.
Please be aware that suppliers will be required to submit scientific validations of their interventions, for review and approval prior to being allowed to provide the product to our stores and clubs. It should also be noted that the microorganisms used for validations must be indicative of enteric pathogens and APC counts will not be accepted.
Suppliers are responsible for ensuring all sites providing product to Walmart retail operations are compliant with all federal, state, and local requirements. In addition, all products provided to Walmart must be compliant with the federal, state, and local requirements for the store/club in which the products will be sold. This may include, but is not limited to, USDA or FDA registration of your facility, product labeling requirements, etc.
Suppliers (both domestic and foreign) are also expected to assist regulatory and health agencies with investigations in a timely manner. Walmart assists various regulatory agencies in outbreak investigations and expect suppliers to provide any traceback documentation that may be requested. Likewise, if public health may be at risk, even if your product has not been directly implicated in an outbreak, it is our expectation that suppliers comply with any recommended product removals.
If for any reason a situation arises where you need to remove product from Walmart Stores, Sam’s Clubs, Distribution Centers, or Fulfillment Centers:
- Contact your Buyer and your Food Safety Manager immediately to communicate that a removal is necessary. For any impending recalls impacting Walmart and/or Sam’s Club, it is important that this contact be made prior to any public notification. Additional information may be requested, which must be provided in a timely manner.
- The Walmart Recall Managers will take the lead in initiating the recall, communicating to all impacted stores, clubs, distribution centers, and fulfillment centers to hold or remove product quickly. They will also send communications to our members and online customers notifying them of a potential issue. Once a recall is terminated and you have approval, you may resume sending safe products to our stores, clubs, distribution centers, and fulfillment centers.
- Recall information, based on manufacturers’ and regulatory agencies’ press releases that involve products sold through Walmart stores, Walmart.com, Sam’s Club, or SamsClub.com can be found here.
Retail Link® is an online hub for the data, documentation, reports, and special applications that suppliers use to manage their business with Walmart. The Product Removal app is located within Retail Link® and is used to remove products from stores, clubs, distribution centers and fulfillment centers. The Walmart Food Safety & Health compliance team uses data to execute product withdrawals and recalls through this portal.
While it is an expectation that all suppliers have a complaint management program in place, Walmart has specific expectations of suppliers who provide unlabeled product to our stores and/or clubs. Walmart expects these suppliers to react with haste and launch a thorough investigation anytime a food safety related complaint is received. Food Safety related complaints may include (but are not limited to) issues involving:
- Illness
- Injury
- Death
- Foreign Objects
- Chemical Taste/Odor
- Alleged food tampering originating at the supplier or within their supply chain
- Any of the above issues resulting in Medical Attention being sought
- Any of the above issues resulting in Legal Action
- Any of the above issues resulting in escalation through Media or Social Media
Food safety complaints should be handled with the upmost priority. Suppliers should acknowledge receipt of any escalated complaint sent to them directly from a Food Safety Manager within 24 hours. We recognize that some complaints may require more time to investigate than others, however, we do expect an investigation report be submitted back to the Food Safety Manager within the requested timeline. If no timeline is provided, this information should be provided no later than two weeks from initial receipt of the complaint. Information expected to be included in the report can be found in the Investigation Expectations section below.
Because you as the supplier are ultimately responsible for any legal or financial outcomes from the compliant or claim, Walmart asks that you contact the customer/member directly in order to obtain any additional information you may need in order to conduct your investigation. All communications with the customer/member should be handled in English, or the customer’s/member’s preferred language, during reasonable hours for the U.S. and in the form of communication that is most comfortable for the customer/member (email/phone). The supplier can determine if they prefer to handle these communications internally or utilize a third-party customer service agency (which may be preferred by international suppliers.) All communications should be initiated with the customer/member within 48 hours of receiving the complaint. For this reason, we ask all suppliers to have an emergency plan in place to cover issues that may arise during weekends or holidays.
If you need to retrieve the product, packaging, or foreign object for analysis we request that suppliers send a pre-paid shipping container with a tracking number to the customer/member. We recommend international suppliers partner with a third-party company or lab to send and receive these pre-paid trackable shipping containers for expedited investigations. If the complaint could result in legal action, suppliers should consider having the pre-paid trackable shipping container sent directly to a third-party lab for investigation to maintain chain-of-command and to ensure final analysis results are free of bias which will present better in a legal setting.
If at any time during your investigation of an issue you find that there may be a widespread issue which could impact additional customers/members, suppliers should immediately contact the Food Safety Recall team to begin a product removal. (See Product Removals section above.)
A summary of each area below should be included in the investigation report that is submitted back to your Food Safety Manager upon their request (as applicable). Please ensure the facility name and address is clearly indicated on each investigation report unless it cannot be determined from the complaint information provided.
- Analyzing Similar Complaints: In order to determine if the complaint is an isolated incident or a potential widespread food safety issue, we ask that you analyze other complaints received in the previous 6 months (this timespan can be expanded or contracted based on the shelf-life of the product.) If you have received similar complaints for the implicated item, products that are similar to the implicated item, or products that are made with the same raw materials as the implicated item, we ask that you inform your Food Safety Manager immediately. In an event that you should notice a trend, we may need to take additional actions. Data should be normalized for this analysis.
- Review of Production Records: If a lot code for the product is available, suppliers are expected to trace the lot back to the product date and review records for any abnormalities. This includes, but is not limited to, batch sheets, finished product testing results, foreign object detection equipment records (e.g. for metal detectors, x-ray, optical sorters, etc.) including calibration logs and any detection issues/rejections, notice of unusual occurrences and corrective action logs (NUOCA), deviation logs, cleaning and sanitation logs, and/or any other relevant CCP records.
- Review of Retain Samples: Retain samples should be analyzed to determine if the reported issue can be observed in similar products. Where invasive tests are required, we recommend documenting the tests via testing records and photographs.
- Review of Production Room CCTV: Where relevant and useful, review production day CCTV footage to help determine complaint cause.
- Conducting the Root Cause Analysis: A formal root cause analysis should be conducted for the complaint using all available information. The root cause analysis should consider any additional products or lots that could be affected by the issue. If you do not have a root cause method defined in your SOP, use the questions who, what, when, where, why, and how to narrow in on one key issue.
- Creating & Implementing Corrective and Preventive Actions: Corrective actions should be identified/implemented and preventive actions taken that are designed to mitigate or prevent the risk of the same issue occurring. A formal timebound corrective action report should be submitted to your Food Safety Manager for review and approval. Depending on the situation, it may be acceptable to implement both short-term and long-term corrective actions. For critical food safety issues identified, immediate corrective actions are to be completed within 24 hours, or prior to further production.
- Confirmation of Resolution with Customer/Member: Unless the customer/member has explicitly indicated that do not wish to be contacted, or no contact information is provided, suppliers should contact the customer/member to obtain additional information as well as to resolve the issue. Please always treat the customer/member with respect, show empathy regarding their recent food safety complaint issue, and keep a detailed record of these communications.