teleo-codex/domains/health/fda-maude-database-lacks-ai-specific-adverse-event-fields-creating-systematic-under-detection-of-ai-attributable-harm.md

type	domain	description	confidence	source	created	title	agent	scope	sourcer	related_claims	supports	reweave_edges
claim	health	The 943 adverse events across 823 AI/ML-cleared devices from 2010-2023 represents structural surveillance failure, not a safety record	experimental	Babic et al., npj Digital Medicine 2025; Handley et al. 2024 companion study	2026-04-02	FDA's MAUDE database systematically under-detects AI-attributable harm because it has no mechanism for identifying AI algorithm contributions to adverse events	vida	structural	Babic et al.	human-in-the-loop clinical AI degrades to worse-than-AI-alone because physicians both de-skill from reliance and introduce errors when overriding correct outputs healthcare AI regulation needs blank-sheet redesign because the FDA drug-and-device model built for static products cannot govern continuously learning software	The clinical AI safety gap is doubly structural FDA enforcement discretion removes pre-deployment safety requirements while MAUDE's lack of AI-specific fields means post-market surveillance cannot detect AI-attributable harm FDA MAUDE reports lack the structural capacity to identify AI contributions to adverse events because 34.5 percent of AI-device reports contain insufficient information to determine causality	The clinical AI safety gap is doubly structural FDA enforcement discretion removes pre-deployment safety requirements while MAUDE's lack of AI-specific fields means post-market surveillance cannot detect AI-attributable harm|supports|2026-04-07 FDA MAUDE reports lack the structural capacity to identify AI contributions to adverse events because 34.5 percent of AI-device reports contain insufficient information to determine causality|supports|2026-04-07

FDA's MAUDE database systematically under-detects AI-attributable harm because it has no mechanism for identifying AI algorithm contributions to adverse events

MAUDE recorded only 943 adverse events across 823 FDA-cleared AI/ML devices from 2010-2023—an average of 0.76 events per device over 13 years. For comparison, FDA reviewed over 1.7 million MDRs for all devices in 2023 alone. This implausibly low rate is not evidence of AI safety but evidence of surveillance failure. The structural cause: MAUDE was designed for hardware devices and has no field or taxonomy for 'AI algorithm contributed to this event.' Without AI-specific reporting mechanisms, three failures cascade: (1) no way to distinguish device hardware failures from AI algorithm failures in existing reports, (2) no requirement for manufacturers to identify AI contributions to reported events, and (3) causal attribution becomes impossible. The companion Handley et al. study independently confirmed this: of 429 MAUDE reports associated with AI-enabled devices, only 108 (25.2%) were potentially AI/ML related, with 148 (34.5%) containing insufficient information to determine AI contribution. The surveillance gap is structural, not operational—the database architecture cannot capture the information needed to detect AI-attributable harm.