Z-2205-2024 Class II Ongoing

Recalled by Medtronic Inc. — Mounds View, MN

Recall Details

Product Type
Devices
Report Date
July 3, 2024
Initiation Date
April 16, 2024
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
13 units

Product Description

MIRRO MRI VR SureScan, Model Number DVME3D4, Implantable Cardioverter Defibrillator

Reason for Recall

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

Distribution Pattern

Worldwide - US Nationwide distribution in the states of CA, CT, FL, IN, MA, MI, NC, NH, NJ, NM, NY, OH, TX, VA and the countries of Australia, Austria, Bulgaria, Canada, China, Croatia, Czech Republic, France, Georgia, Germany, Greece, Guadeloupe, Iceland, Ireland, Italy, Jordan, Kosovo, Latvia, Moldova, Republic Of, Netherlands, Northern Ireland, Norway, Oman, Panama, Poland, Portugal, Qatar, Reunion, Slovakia, Slovenia, Spain, Sweden, Switzerland, United Arab Emirates, United Kingdom.

Code Information

GTIN: 00763000611989, Serial Numbers: CWR621520S, CWR621521S, CWR621522S, CWR621523S, CWR621524S, CWR621525S, CWR621526S, CWR621527S, CWR621528S, CWR621529S, CWR621530S, CWR621531S, CWR621532S.