Medtronic Recalls
157 recalls on record · November 11, 2015 to May 6, 2026 · Medical Devices
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 6, 2016Medical DevicesFDA
Medtronic Inc. recalls Reveal LINQ insertable Cardiac Monitor, Model LNQ11. Monitors subcutaneous ECG continuously.
Hazard: Medtronic has identified an issue with the sensitivity of an algorithm used in the Reveal LINQ ICM that may prematurely trigger the Recommended Replacement Time (RRT) alert in some devices. Battery capacity is not affected and the device will continue to support data collection and manual data transmissions. As part of the normal behavior of the device, 30 days after RRT status is reached, Reveal
February 24, 2016Medical DevicesFDA
Medtronic recalls Best Practice Kits containing certain production lots of Endo GIA Ultra Universal Stapler Handles Product Usage: The
Hazard: Staplers fail to fire or partially fire and reports of the instrument articulating lever disengaging during use
February 24, 2016Medical DevicesFDA
Medtronic recalls Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Ref: EGIAUXL Product Usage: The Endo GIA Ultra Universal
Hazard: Staplers fail to fire or partially fire and reports of the instrument articulating lever disengaging during use
February 24, 2016Medical DevicesFDA
Medtronic recalls Covidien Endo GIA Ultra Universal Standard Stapler Handle Ref: EGIAUSTND Product Usage: The Endo GIA Ultra Universa
Hazard: Staplers fail to fire or partially fire and reports of the instrument articulating lever disengaging during use
February 24, 2016Medical DevicesFDA
Medtronic recalls Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Ref: EGIAUSHORT Product Usage: The Endo GIA Ultra Uni
Hazard: Staplers fail to fire or partially fire and reports of the instrument articulating lever disengaging during use
December 9, 2015Medical DevicesFDA
Medtronic Inc. recalls Medtronic InSync III, model 8042, 8042B and 8042U. Implantable pulse generator pacemaker.
Hazard: Medtronic has confirmed an issue with InSync III CRT-pacemaker devices related to long-term battery performance. The root cause is unexpected high battery impedance.
November 11, 2015Medical DevicesFDA
Medtronic Inc. recalls Medtronic Achieve Cables, model 990066. The sterile, single use only Electrical Cable (Model 990066) provides the condu
Hazard: 64 units of Achieve Electrical Cables were shipped with a potential sterility breach.