Here we propose a dual scoreboard, comprised of leading and lagging statistics taken from actual operations and the system’s output — as expressed through recall and outbreak incidents. The work is the first application of the concepts on top of a tier approach to supplier risk employed throughout a multi-supplier grocery distribution system and presented as a launch pad for further industry and regulatory comment.
This series examines food safety as business infrastructure: the business decisions, governance structures, and operational conditions that determine whether technical food safety systems can hold under production pressure. The first three articles followed the record inward—from the corrective-action log, through the cost of repetition, to what growth asks a system to carry. This article follows that same operational reality outward.
Dr. Justin Ransom, administrator of the U.S. Department of Agriculture’s (USDA) Food Safety and Inspection Service (FSIS) will present at this year’s Food Safety Consortium Conference October 21-23 in Washington DC along side, Dr. Donald A. Prater, Acting Deputy Commissioner for Food, FDA.
New award will recognize food and beverage organizations applying innovative technology to strengthen food safety performance
FSTR is being launched in conjunction with its anchor research study: The Food Safety Digital Maturity Benchmark, giving food manufacturers an independent way to measure the impacts of digital transformation, technology adoption, and operational performance. The study findings will debut at the 15th Anniversary Food Safety Consortium Conference & Expo, October 21-23, in Washington DC.
The term, Normalization of Deviance has since become standard vocabulary in aviation safety, nuclear safety, and patient safety literature, precisely because the pattern keeps recurring: a known risk, documented, unresolved, tolerated because the bad outcome hasn’t happened yet… until the day it does.
HHS proposed a rule requiring manufacturers to notify the FDA when concluding that the use of a substance added to human or animal food is GRAS and, alongside the USDA, submitted for final review the federal government’s first proposed definition of ultra-processed foods (UPFs). Critics complain that while the GRAS rule would require manufacturers to notify the FDA when they determine a new food substance is GRAS, manufacturers would still self-determine that safety conclusion themselves. Substances introduced into the market before the regulations go into effect, would be eligible for a separate, time-limited streamlined submission pathway.
The FDA is implementing a major reorganization plan called “Simple Reform” on October 1, 2026, which shifts field inspectors from specialized product roles back to generalist investigators and centralizes administrative functions. The food and beverage industry should expect a shift in audit dynamics, meaning audits will likely focus less on highly specific, niche technical processes and more on foundational, broad-spectrum quality systems. Dr. Stephen Ostroff and Frank Yiannas, both former Deputy Commissioners at FDA offer their opinions on Simple Reform.
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.
