Ethicon Recalls Physiomesh Hernia Repair Implant Due to High Failure Rate
Physiomesh Injury Attorneys
Johnson & Johnson subsidiary Ethicon recalled Physiomesh Flexible Composite Mesh after two large studies revealed high revision rates. Physiomesh is implanted laparoscopically to repair ventral hernias. The studies found that patients implanted with Physiomesh experienced complications which required revision surgeries to fix problems associated with the implanted device. Complications associated with Physiomesh include infection, persistent pain, intestinal blockage, mesh migration, mesh shrinkage, and hernia recurrence.
If you or someone you know received an Ethicon Physiomesh Flexible Composite Mesh implant to repair a ventral hernia and have suffered a serious injury, contact us. Our product liability attorneys have litigated thousands of claims against medical device manufacturers and can advise you of your legal rights and options.