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Ethicon Mesh Products

Devices involved in litigation.

Physiomesh Flexible Composite

RECALLED 2016

Recalled due to higher rates of hernia recurrence and reoperation. Subject of MDL 2846.

Prolene Hernia System

Active Claims

Polypropylene mesh system linked to chronic pain, infection, and mesh migration.

Proceed Surgical Mesh

Active Claims

Multi-layer mesh with reports of adhesions, pain, and revision surgery requirements.

Ultrapro Hernia System

Active Claims

Lightweight partially absorbable mesh with reported complications.

Physiomesh Recall

In May 2016, Ethicon voluntarily recalled Physiomesh after data revealed higher rates of hernia recurrence and revision surgery compared to competitor products. Over 20,000 claims have been filed in MDL 2846.

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FDA Class I Recall - Ethicon Physiomesh May 2016

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