Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0407-2019 — Medtronic CareLink Encore 29901 Programmer

U.S. FDA — Device Enforcement · United States · 2018-10-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0407-2019
Date of alert
2018-10-02
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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