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The FDA is calling on healthcare facilities to immediately implement employee training for updated reprocessing instructions for two Olympus duodenoscope models. Read More
Cook Medical is recalling 360 specific lots of single lumen central venous catheters and pressure monitoring sets and trays due to catheter tip fracture and/or separation. Read More
Wayne, Pa.-based Teleflex is recalling 47,140 units of its Arrow International intra-aortic balloon pump catheters and percutaneous insertion kits following reports of serious adverse events. Read More
A board working on a nationwide system to monitor the risks and benefits of medical products on the market outlined some of the projects it hopes to undertake to help boost the safety and effectiveness of devices. Read More
Brainlab is recalling its cranial image-guided surgery system due to potential inaccuracies in the display compared with a patient’s anatomy. Read More