The FDA has announced two Medtronic MiniMed insulin pump recalls; one due to a potentially damaged retainer ring which can cause serious injuries or death, and another involving remote controllers…
Medtronic is recalling about 9,000 devices used to treat brain aneurysms following reports of serious injuries and deaths due to the delivery system fracturing and leaving sharp debris in patients'…
An investigation into a tuberculosis outbreak linked to FiberCel bone matrix products has resulted in the CDC recommending any patients who received the bone product undergo full tuberculosis treatment.
Medtronic must face a product liability lawsuit filed on behalf of a woman who suffered worsening spasticity and pump failures and had to have the device replaced twice due to…
A new study reveals the recently recalled Medtronic Heartware HVAD system has more than double the risk of causing neurological adverse events in patients than the Abbott Heartmate3, which is…
The FDA says problems with Medtronic Heartware HVAD implants, which resulted in its removal from the market, put patients at risk of severe injury or death.
A new report indicates the FDA and Medtronic knew of HeartWare implant problems and deaths for years, but took little action to make the devices safer and kept allowing them…
Medtronic faces a product liability over its recalled Minimed infusion pumps filed by a man who says defects in the device caused him to suffer hyperglycemia.
The CDC is investigating an outbreak of tuberculosis linked to recalled FiberCel bone products.
After issuing a series of Class I recalls for HeartWare HVAD systems over the past decade, Medtronic has announced that it will remove the cardiac devices from the market, as…