medical device recall

Actavis Fentanyl Transdermal System 25 mcg/hour C-II Patch Recall Issued By Actavis Over Potential Release Of Active Ingredients Faster Than Approved Laboratory Testing Specification

Recalls & Recalled Products

Actavis Recalls 18 lots of Fentanyl Transdermal System 25 mcg/hour C-II Patches Over Risk Of Release Of Active Ingredient Faster Than Approved Specification in Lab Testing. A medical patch recall has been issued by Actavis Inc. (Actavis”) recalling 18 lots of Fentanyl Transdermal System 25 mcg/hour C-II patches manufactured for Actavis by Corium International in [...]

Medtronic Octopus Nuvo Tissue Stabilizer Class I Recall Issued By Medtronic Over Potential Fragments & Heart Tissue Damage

Recalls & Recalled Products

Medtronic Recalls Octopus Nuvo Tissue Stabilizer Over Potential Fracturing of Surgical Device Component That Could Potentially Cause Heart Tissue Damage. A class I surgical device recall has been issued by Medtronic, Inc. (Medtronic”) recalling approximately 571 Medtronic Octopus Nuvo Tissue Stabilizers distributed to healthcare facilities reportedly because a component of the Medtronic Octopus Nuvo Tissue [...]

Medtronic Sprint Fidelis Leads Recall Settlement Of Personal Injury Lawsuits

Recall Settlements

Medtronic Agrees To Pay $268 Million To Settle Personal Injury Recall Lawsuit Claims Against Medtronic Over Recalled Medtronic Sprint Fidelis Leads. A settlement has been reached in a mass tort personal injury recall lawsuit against Medtronic, Inc. (“Medtronic” or “Defendant”), alleging among other things that the recalled Medtronic Sprint Fidelis leads (i.e., wires or cables [...]

DePuy Orthopaedics Recall Lawsuit Complaint Filed Over Recalled DePuy ASR Hip Replacement System

Recall Lawsuits

DePuy Orthopaedics DePuy ASR Acetabular Hip Replacement Patients File Personal Injury Recall Lawsuit Against DePuy Orthopaedics Over Recalled DePuy ASR Hip Replacement System. A personal injury recall lawsuit has been filed against DePuy Orthopaedics, Inc. (“DePuy Orthopaedics”) and Chesapeake Surgical, LTD (“Chesapeake Surgical”) in the Circuit Court for Prince George’s County, Maryland (Civil Action Case [...]

CareFusion Alaris PC Unit Model 8015 Medical Device Recall Issued Over Alleged Alaris Communication Errors

Recalls & Recalled Products

CareFusion Recalls Alaris PC Unit Model 8015 Medical Device Over Alleged Alaris Communication Errors. A class I recall has been issued by CareFusion Corporation (“CareFusion”), 10020 Pacific Mesa Boulevard, San Diego, California 92121, recalling Alaris PC Unit Model 8015, an electronic infusion pump that delivers controlled amounts of medications or other fluids to patients through [...]