Ranks distinct AI gain and problem claims from the published record. Scores reward impact, independent source strength, scale, confidence, and recency.
On June 13 2025, Crime Science published a systematic literature review of AI and NLP for online fraud detection. The authors screened 2457 records and analyzed 223 studies, mapping data sources, algorithms, and evaluation metrics across 16 fraud types and summarizing best-performing methods for detecting scams in text.
Published March 2024, this peer-reviewed article analyzes automated systems used in public decision-making for migration, asylum and mobility. It finds that GDPR and AI Act definitions centered on fully automated decisions miss common practices where systems assist human decision-makers, and it proposes a taxonomy to support fundamental rights analysis.
In an online cross-sectional study in France with 204 general practitioners and 942 patient histories, researchers compared AI to physicians in recording histories during initial consultations across categories such as chronic disease, surgical, obstetric, occupational, allergies, and family cancer history.
The paper reviews persistent bottlenecks in moving evidence-based interventions into routine care and describes how data science and AI methods can help extract and synthesize implementation materials, analyze context, and support stakeholder engagement and adaptation, illustrated with a live precision oncology project and the ImpleMATE platform.
On 2026-06-23, an FDA device event record for Davinci xi by Intuitive surgical, inc. cited a literature case report on AI for surgical support in robot-assisted distal pancreatectomy. The record states the dissection line on the lower margin of the pancreas was falsely recognized and pancreatic tissue was damaged during the procedure.
Ossur recalled its Rheo Knee bionic prosthetic after an internal audit found units were released for distribution without fully going through the assembly process. The device is described as using Artificial Intelligence to adapt to walking style and environment for lower extremity amputations, and customers were told on February 26, 2015 to return units for acceptance testing.
The FDA received a malfunction report for the Reveal LINQ implantable cardiac monitor made by Medtronic europe sarl. The report describes false pause episodes due to undersensing and a customer concern that the device's AI algorithm adjudicated episodes the customer considered true pauses as false. The device remains implanted.
The FDA received a malfunction report for the Accurhythm za420 (pause) device made by Medtronic, inc. The report stated that the device's artificial intelligence algorithm rejected true pause episodes as false. The source notes that no patient complications have been reported as a result of this event.