FDA MedWatch - Cardiac Resynchronization Therapy with Defibrillation (CRT-Ds) and Implantable Cardiovert-Defibrillators (ICDs) by Medtronic: Class I Recall- Manufacturing Error Preventing Electrical Shock Delivery

If your email program has trouble displaying this email, view it as a web page

MedWatch - The FDA Safety Information and Adverse Event Reporting Program Cardiac Resynchronization Therapy with Defibrillation (CRT-Ds) and Implantable Cardiovert-Defibrillators (ICDs) by Medtronic: Class I Recall- Manufacturing Error Preventing Electrical Shock Delivery AUDIENCE: Risk Manager, Cardiology, Surgery, Patient ISSUE: Medtronic is recalling certain ICDs and CRT-Ds due to a defect in the manufacturing process.  This defect causes an out of specification gas mixture inside the device and may prevent the device from delivering the electrical shock needed to pace a patient's heartbeat or revive a patient in cardiac arrest. The delay or inability to deliver a shock to a patient in cardiac arrest or pace a patient's heart whose heartbeat is too slow could result in serious injury and/or death. Product Codes: NIK, LWS Serial Numbers: See Complete List in Recall Notice Manufacturing Dates: July 13, 2013 to August 8, 2017 Devices Recalled in the U.S.: 48 units nationwide BACKGROUND: Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) are devices that provide pacing for slow heart rhythms, and electrical shock or pacing to stop dangerously fast heart rhythms. RECOMMENDATION: On January 22 2018 Medtronic sent an Urgent Medical Device Recall notice to affected customers. The notice asked customers to: Consider Prophylactic device replacement for patients who have been implanted with one of the affected devices. Contact their Medtronic sales representative for terms and conditions for device warranties. Review the recall notice and ensure appropriate staff is aware of the notice. Medtronic will offer a supplemental device warranty for affected devices. Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program: Complete and submit the report Online: www.fda.gov/MedWatch/report Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178 Read the MedWatch Safety Alert, including a link to the recall notice, at: https://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm598446.htm

U.S. Food and Drug Administration 10903 New Hampshire Avenue, Silver Spring, MD 20993 1-888-INFO-FDA (1-888-463-6332) Privacy Policy | www.fda.gov Manage Preferences or Unsubscribe from this List | Unsubscribe from all Email Lists