FDA Device recall Z-0406-2019
Medtronic CareLink 2090 Programmer
- FDA Device
- Class II
- ongoing
- Published 2018-11-14
On 2018-11-14 the FDA classified a Class II recall of Medtronic CareLink 2090 Programmer by Medtronic Cardiac Rhythm And Heart Failure Crhf, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0406-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2018-10-02 |
| Published | 2018-11-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medtronic Cardiac Rhythm And Heart Failure Crhf |
| Distribution | n/a |
Product
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.
Identifiers
| code_info | All Serial Numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0406-2019%22
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