FDA Enforcement Class II Ongoing

Medtronic CareLink 2090 Programmer

Recall: Z-0406-2019 · Reported November 14, 2018

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Enforcement

Recall Number
Z-0406-2019
Event ID
81300
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
November 14, 2018
Initiation Date
October 2, 2018
Classification Date
November 8, 2018
Address
8200 Coral Sea St Ne, Mounds View, MN, 55112-4391, United States

Description

Medtronic CareLink 2090 Programmer

Reason

Vulnerabilities have been identified in the SDN download process that may allow an individual with malicious intent to update the programmers with non-Medtronic software during an SDN download.

Code Info

All Serial Numbers

Distribution

Worldwide

Quantity

30172 units