Abbott Medical: Medical Device Recalls in 2025

According to to data from the FDA, there were 4 medical device recalls made by Abbott Medical in 2025. See the details of the recalls below.

You can see similar recalls for other firms.

• Aveir DR Leadless Pacemaker (LP) Ventricular Device REF LSP202V UDI-DI code: 05415067040725 REF LSP112V UDI-DI code: 05415067034472 The Aveir leadless pacemaker system supports the implantation and use of an Aveir Leadless Pacemaker (LP) within the targeted chamber(s) of the heart for monitoring a patient s heart rate and providing rate responsive bradycardia pacing therapy to regulate heart rate.
• The Merlin PCS 3650 programmer Model 3330 The Merlin PCS programmer model 3650 is a portable, dedicated programming system which operates using the Merlin PCS Model 3330 software and is designed to interrogate, program, display data from, and test Abbott Medical implantable devices and leads.
• Eterna SCS IPG (Implantable Pulse Generator), Model Number 32400
• Liberta RC DBS IPG (Implantable Pulse Generator), Model Number 62400