MassDevice7h
Smiths Medical has a serious recall involving vein access ports
The FDA has labeled Smiths Medical's recall of ProPort Implantable Plastic Port as Class I, the most serious kind.
Medtronic recalls aneurysm-treating device linked to four deaths
The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.
MedTech Dive1d
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 ...
Medical Device Network on MSN1d
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 ...
MassDevice2d
Medtronic recalls embolization device after reported deaths
The FDA deemed a recall of some Medtronic Pipeline Vantage embolization devices serious after multiple deaths related to the ...
Medtronic slips after FDA notice on product recall (update)
Shares of Medtronic (NYSE:MDT) reached a session low on Tuesday after the U.S. Food and Drug Administration (FDA) announced a ...
FDA issues Medtronic embolization device recall and correction notice
In a notice posted to the agency’s website, the FDA noted that on January 30, 2025, Medtronic (MDT) Neurovascular sent all affected customers ...
Endovascular Today2d
Medtronic Recalls Pipeline Vantage 027, Updates IFU for Pipeline Vantage 021
The FDA announced that Medtronic initiated a device recall and correction for embolization devices. The FDA has identified ...
MedTech Dive2d
Top device firms report safety data late: BMJ
BD, Medtronic and Abbott were among the top 10 device companies with the highest number of late reports to the FDA, the study ...
JD Supra3d
State Licensing Spotlight – Prescription Medical Device Manufacturers & Distributors: Enforcement and penalties for operating without a license
The regulatory environment for prescription medical device manufacturers and distributors has become increasingly stringent as state-based ...
Will ISRG Stock Drop Continue After da Vinci 5 Recall?
Intuitive Surgical faces a Class 2 recall for its da Vinci 5 system due to a pedal issue. Will this affect its 2025 rollout?
Insurance Business America4d
Australian product recalls climb amid regulatory changes – Sedgwick
Product recalls across key Australian industries increased by 14% in the second half of 2024 compared to the first half, ...