Recalls · Brand

Medtronic Inc., Cardiac Rhythm and Heart Failure recalls

Every recall we track for Medtronic Inc., Cardiac Rhythm and Heart Failure — 2 in all, all from 2017 — plus the complaints and injury reports the public filed about them.

2recalls

Recalls per year, by danger level

2 recalls since 2017.

All FDA recall records for Medtronic Inc., Cardiac Rhythm and Heart Failure since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.

Recalls per year for Medtronic Inc., Cardiac Rhythm and Heart Failure, by danger level
Year	Use caution	Total
2017	2	2
2018	0	0
2019	0	0
2020	0	0
2021	0	0
2022	0	0
2023	0	0
2024	0	0
2025	0	0
2026 (to date)	0	0

What to do if you have a recalled Medtronic Inc., Cardiac Rhythm and Heart Failure product

Match the model, catalog or lot number on your device to the recall.
Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
Report problems to FDA MedWatch.

See this week’s new recalls.

All Medtronic Inc., Cardiac Rhythm and Heart Failure recalls

1 shown

Use cautionMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure recalls MyCareLink Smart Patient Monitors. It is intended for use with a compatible Medtronic patient implanted heart device.
Medtronic recalls MyCareLink Smart Patient Monitors used with implanted heart devices. These monitors may miss critical heart device alerts, risking missed CareAlert notifications for patients with two or more implanted devices.
MedtronicJul 14, 2017

Medtronic Inc., Cardiac Rhythm and Heart Failure recall questions

How many recalls has Medtronic Inc., Cardiac Rhythm and Heart Failure had?

2 recalls from Medtronic Inc., Cardiac Rhythm and Heart Failure are on record with U.S. safety agencies, from 2017.

What is the most recent Medtronic Inc., Cardiac Rhythm and Heart Failure recall?

Medtronic Inc., Cardiac Rhythm and Heart Failure recalls MyCareLink Smart Patient Monitors. It is intended for use with a compatible Medtronic patient implanted heart device., dated Jul 14, 2017. Every Medtronic Inc., Cardiac Rhythm and Heart Failure recall is listed on this page, newest first.

What should I do if I have a recalled Medtronic Inc., Cardiac Rhythm and Heart Failure product?

Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.

How do I get alerts for new Medtronic Inc., Cardiac Rhythm and Heart Failure recalls?

Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.