In May 2016, Johnson & Johnson subsidiary Ethicon issued a recall of its Physiomesh Flexible Composite Mesh used in hernia repair surgeries after data from two European hernia registries indicated the product was associated with high revision rates. In an Urgent Field Safety Notice distributed to surgeons and operating room supervisors, Ethicon said the review …. Read More
Tag Archives: Ethicon Recall Claims
Free Case Evaluation
If you or a loved one experienced complications from a hernia mesh device please contact us by submitting the form, or by calling us at
so we can confidentially discuss the legal options that may be available to you. Fields marked with * are required.