American Hospital Association48m
FDA issues recall on Medtronic embolization devices
The Food and Drug Administration has identified a Class I recall of Medtronic Neurovascular 027 Compatible Pipeline Vantage ...
Modern Healthcare6h
FDA deems Medtronic’s Pipeline Vantage recall ‘most serious’
The recall, which affects two models of Pipeline Vantage embolization devices, is linked to 17 injuries and four deaths.
MedTech Dive6h
Monogram robot wins FDA OK; Vicarious hit by supplier woes
Monogram Technologies secured 510(k) clearance for its robotic knee replacement system, while Vicarious Surgical blamed ...
FDA tags Medtronic embolisation device recall as Class I
Medtronic initiated the recall of certain Pipeline Vantage embolisation devices in January 2025 following reports of four ...
The Healthy @Reader's Digest on MSN10h
An Acne Treatment Has Been Recalled by a National Retail Chain
Customers are urged to “immediately discontinue use” of this popular acne product, despite rave reviews for its effectiveness ...
Medtronic recalls embolization devices tied to 17 injuries, 4 deaths
Medtronic will remove one model of Pipeline Vantage devices from where they’re used and sold and will update the instructions ...
ET HealthWorld11h
FDA classifies recall of Medtronic embolization devices as 'most serious'
The recall impacts the Pipeline Vantage devices compatible only with 0.027" inner diameter microcatheters, Medtronic said.
FOX 13 Tampa Bay on MSN21h
6 popular acne treatment products recalled for elevated levels of benzene
The FDA has recalled six popular acne treatment products due to elevated levels of benzene. Experts say that some exposure to ...