Covidien now faces a growing number of surgical stapler class action lawsuits in Canada, which are nearly identical to those being filed in the U.S. over complications and failures following…
A Covidien surgical stapler which broke during surgery led to a man suffering severe injuries requiring a colostomy, according to a recently filed product liability lawsuit.
The FDA is warning that Medtronic leadless pacemakers could increase the risk of cardiac perforations, resulting in life-threatening complications.
Medtronic now faces a class action lawsuit in Canada over problems with its MiniMed 600 series insulin pumps, which have been subject to various recalls in recent years due to…
A product liability lawsuit claims a man suffered numerous complications, including sepsis, following the failure of surgical staples used in his abdomen.
The findings of a new study indicate leadless pacemakers have a lower rate of complications than older implants which require wired leads be implanted in the heart.
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…