Raw food safety data is most valuable when paired with actionable insights. By replacing manual workflows with automated software, food manufacturers can unlock real-time trend analysis and identify contamination hot spots before they spread.
FDA sent a letter to the infant formula industry and their supply chain partners highlighting multiple recent public health events where risks were introduced through the supply chain and to call for increased vigilance by industry to ensure the safety of ingredients and finished infant formula products.
Fifteen years of preventive controls investment has produced a record detailed enough to answer a question most operations confront only under pressure: not whether a system performs, but whether it can carry what growth asks of it. Rising volume, added complexity, new customers, and shifting requirements all impact the same structure, and they reveal whether the structure was built to absorb them, or whether people have been absorbing the difference on its behalf. This five-part series examines food safety through the business realities leaders already navigate: profitability, risk, growth, brand trust, and organizational function.
Many food manufacturers treat supplier verification as a filing exercise collect the certificate of analysis, confirm it’s in spec, move on. This article argues that approach satisfies neither FSMA’s supply-chain program nor the scrutiny of a recall. It explains what 21 CFR Part 117 Subpart G actually requires (risk-based verification scaled to hazard severity), why a COA is an assertion rather than proof of safety, and how to build a verification program independent testing, representative sampling, and documented reasoning that matches the hazard rather than just collecting paperwork.
On June 15, 2026 The FDA held a public meeting to give the public an opportunity to share information on continued implementation of the Food Traceability Rule and areas of remaining concern, specifically as they relate to lot-level tracking and flexibilities for compliance
FDA announced a list of guidance topics includes possible new topics for guidance documents or revisions to existing guidance documents that the FDA’s Human Foods Program is considering, including Food Chemical Safety, Dietary Supplements, and Innovation and Microbiological Food Safety.
Growth, continuous improvement, and increased throughput should never come at the expense of robust food safety practices. Instead, food safety programs must evolve alongside manufacturing operations to ensure both objectives advance together. The challenge arises when operational excellence begins to outpace the food safety systems designed to protect both consumers and brands.
Pests hide wherever food residue, moisture, warmth and access points converge. In food processing facilities, those conditions appear every day in loading docks, floor drains, equipment voids and ingredient storage. A proactive Integrated Pest Management (IPM) program is the FDA-aligned standard for identifying and eliminating those conditions before they trigger a compliance issue or failed audit
The updated compliance program will focus exclusively on monitoring pesticide residues in foods. To reflect this, the program has been renamed “Pesticides in Human Foods – Domestic and Import.”
New investigation is the first to trace microplastics and plastic chemicals from plastic packaging into baby food. The testing commissioned by Greenpeace International in 2025 found plastic particles in the baby food products of two global consumer goods companies – Danone and Nestlé. The study suggests a link between the type of plastic the pouches are lined with – polyethylene – and some of the microplastics found.
