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Johnson & Johnson is facing lawsuits in two states that allege the company engaged in deceptive marketing claims for “new and revolutionary” surgical mesh used to treat women with pelvic organ prolapse. Read More
Physio-Control has announced a recall of specific lots of its Quik-Combo adult pacing/defibrillation/ECG electrodes and its Red-Pak preconnected system due to possible damage to the wire insulation during the manufacturing process. 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
The FDA has labeled the recall of Cook Medical’s single lumen central venous catheters and pressure monitoring sets and trays as Class 1, meaning it could cause serious injury or death. Read More
B. Braun Medical is voluntarily recalling its Dialog+Hemodialysis systems due to fractures in conductivity sensors that may allow air to come in contact with dialysis fluid, leading to poor blood filtration. Read More