Αποτελέσματα Αναζήτησης
2 Οκτ 2024 · Find out which hernia mesh products have been recalled and why, and how to join the lawsuits against the manufacturers. Learn about the FDA warnings, reviews and enforcement actions related to hernia mesh complications.
- Hernia
During surgery, doctors close tears, often using a hernia...
- Kugel Patch
Bard Davol recalled its Kugel Patch hernia mesh in 2005. The...
- C-Qur Mesh
Two patients had a central breakdown of the mesh at about...
- FAQ
The time it takes to repair a hernia varies from 30 minutes...
- Hernia
Find out which hernia mesh products have been recalled by manufacturers since 2005 and what complications they may cause. Learn about the FDA classifications, recall details and sources of the information.
13 Ιουλ 2023 · The FDA provides guidance on how to report adverse events related to surgical mesh used for hernia repair through MedWatch, the FDA Safety Information and Adverse Event Reporting program. The web page also lists the information to include in the reports, such as mesh specifics, operation details, and problem description.
Find out which hernia mesh devices have been recalled by the FDA or the manufacturers due to safety issues. See the table of recalled mesh products, dates, reasons and statuses updated for 2020.
17 Ιουλ 2023 · The FDA analyzed adverse event reports and research papers to inform patients about the risks and benefits of surgical mesh in hernia repair. The agency continues to monitor the safety of the devices, while medtech companies face product liability claims.
13 Ιουλ 2023 · Learn about the benefits, risks, and alternatives of surgical mesh for hernia repair from the FDA. Find out about the types of hernias, causes, treatment options, and complications.
13 Ιαν 2021 · Class 2 Device Recall Covidien. incorrect device is contained in the package. The packaging label indicates that the device is for left side use, the product inside the package is for right side...
