FDA Class I Device Recalls and Nuclear Verdicts Reshape Med-Mal Risk in 2026
FDA Class I device recalls reached a 15-year peak in 2026 with 44 active campaigns; GAO report GAO-26-107619 documented oversight gaps that…
MICRA, standard of care, expert practice
FDA Class I device recalls reached a 15-year peak in 2026 with 44 active campaigns; GAO report GAO-26-107619 documented oversight gaps that…
Robotic surgical systems generate their own data trail — console event logs, instrument usage records, and training certifications. Plainti…
Failure to recognize and treat sepsis within protocol-defined time windows is one of the leading sources of preventable hospital deaths and…
Missed or delayed diagnosis of acute myocardial infarction in the emergency department remains one of the most consequential and litigated…
FDA Class I device recalls hit a 15-year peak in 2026, with functional failure overtaking manufacturing defects for the first time in five…
When the obstetric team fails to apply the recognized shoulder-dystocia maneuver sequence, the result is often a permanent brachial plexus…
Cosmetic surgery complications generate frequent malpractice inquiries but require careful case screening. The bad-outcome defense is power…
Radiologist misreads of CT scans, MRIs, and chest X-rays generate some of the most preventable diagnostic errors in medicine. The liability…
A federal jury awarded $88 million in Patterson v. Medtronic on August 4, 2026, the first bellwether among 2,500-plus Covidien Symbotex mes…
Telehealth encounters have become a routine feature of American healthcare delivery, and they produce a distinct category of malpractice cl…
Stroke malpractice cases offer something most med-mal files lack: a precise, time-anchored causation framework built around the tPA treatme…
Medication errors harm hundreds of thousands of patients each year in the United States, and liability runs across prescribers, dispensing…