iCast Covered Stent Recall Issued Over Separation Risks
Nearly 80,000 iCast covered stents are being recalled following dozens of reports of the balloon or catheter hub separating from the stent during removal.
Nearly 80,000 iCast covered stents are being recalled following dozens of reports of the balloon or catheter hub separating from the stent during removal.
The JPML has rejected a request to consolidate all Atrium ProLite and ProLoop hernia mesh lawsuits before one judge for pretrial proceedings, saying too few cases have been filed.
The JPML will hear oral arguments late next month over whether to consolidate all Atrium ProLite and ProLoop hernia mesh lawsuits for pretrial proceedings.
Atrium Medical says it opposes consolidating all ProLite and ProLoop hernia mesh lawsuits for pretrial proceedings.
A group of plaintiffs has called for all Atrium ProLite and ProLoop hernia mesh lawsuits to be consolidated before one judge for pretrial proceedings in federal court in Central California.
A federal jury in Chicago has ruled in favor of Atrium Medical in a trial over claims its ProLite hernia mesh is defective and unsterile, leading to infections and the…
The first Atrium C-Qur hernia mesh bellwether trial, scheduled to begin earlier this month, has been resolved, with a second trial yet to be scheduled.
Atrium Medical must go to trial to face claims by a plaintiff who says its ProLite hernia mesh was manufactured in an unsterile environment, resulting in an infection.
The first Atrium C-Qur hernia mesh bellwether trial is now scheduled for July 7, 2021 following delays due to the ongoing pandemic.
The first Atrium C-Qur hernia mesh lawsuit will go to trial next month, and will be held remotely due to the ongoing pandemic.