Medtronic Recalls
157 recalls on record · November 11, 2015 to May 6, 2026 · Medical Devices
Recalls by year
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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.
December 28, 2016Medical DevicesFDA
Medtronic Inc recalls Affinity Fusion" Oxygenator with Integrated Arterial Filter, Affinity Fusion cardiotomy/Venous Reservoir, Perfusion Tu
Hazard: Medtronic is initiating a voluntary product recall for specific lot numbers of the Affinity Fusion¿ Oxygenators with Balance¿1 Biosurface. These are distributed as stand-alone devices, or as a combination unit with the Affinity Fusion Cardiotomy/Venous Reservoir, or as part of tubing packs. Medtronic has identified an out-of-specification condition exhibiting additional plastic (flash) in the arterial sampling port adjacent to the arterial outlet port of the oxygenator.
October 5, 2016Medical DevicesFDA
Medtronic Inc. recalls CareLink iPro Version 1.10, Catalog No. MMT-7340 With data obtained from the iPro2 recorder and blood glucose meter, th
Hazard: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software due to a time stamp error.
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Cylindrical Tip Electrode 28CM Item Code: E278628 The Valleylab Laparoscopic Handset and Elect
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Flat L-Hook Electrode Retractable Item Code: E2784R28ASP The Valleylab Laparoscopic Handset a
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Flat L-Hook Electrode 28cm Item Code: E278428 The Valleylab Laparoscopic Handset and Electrode
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Wire L-Hook Electrode Retractable Item Code: E2783R36ASP The Valleylab Laparoscopic Handset an
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Wire L-Hook Electrode Retractable Item Code: E2783R28ASP The Valleylab Laparoscopic Handset and
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Wire L-Hook Electrode 28CM Item Code: E278328 The Valleylab Laparoscopic Handset and Electrodes
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Wire J-Hook Electrode Retractable 28CM Item Code: E2782R28ASP The Valleylab Laparoscopic Handse
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Wire J-Hook Electrode 28CM Item Code: E278228 The Valleylab Laparoscopic Handset and Electrode
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Curved Spatula Electrode Retractable 28CM Item Code: E2781R28ASP The Valleylab Laparoscopic Ha
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Curved Spatula Electrode 28CM Item Code: E278128 The Valleylab Laparoscopic Handset and Electr
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Straight Spatula Electrode 28CM Item Code: E278028 The Valleylab Laparoscopic Handset and Elec
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Flat L-Hook Electrode 36CM Item Code: E277436 The Valleylab Laparoscopic Handset and Electrode
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Wire J-Hook Electrode 45CM Item Code: E277345 The Valleylab Laparoscopic Handset and Electrode
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Wire J-Hook Electrode 36CM Item Code: E277336 The Valleylab Laparoscopic Handset and Electrodes
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Wire J-Hook Electrode 36CM Item Code: E277236 The Valleylab Laparoscopic Handset and Electrode
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Curved Spatula Electrode 45CM Item Code: E277145 The Valleylab Laparoscopic Handset and Electro
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Curved Spatula Electrode 36CM Item Code: E277136 The Valleylab Laparoscopic Handset and Electro
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Straight Spatula Electrode 36C Item Code: E277036 The Valleylab Laparoscopic Handset and Elect
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic AP Argon Blunt Needle Electrode 28cm Item Code: E258328 The Valleylab Laparoscopic Handset and
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Argon Sharp Needle Electrode 28CM Item Code: E258228 The Valleylab Laparoscopic Handset and Ele
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Argon Modified Flat l Electrode 28CM Item Code: E258128 The Valleylab Laparoscopic Handset and
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Flexible Laparoscopic Argon Blade Electrodes 28CM Item Code: E258028 The Valleylab Laparoscopic
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes 6" Item Code: E25306 The Valleylab Laparoscopic Handset
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes 3" Item Code: E25303 The Valleylab Laparoscopic Handset
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
August 24, 2016Medical DevicesFDA
Medtronic recalls Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes Item Code: E253028 The Valleylab Laparoscopic Handset an
Hazard: Potential for compromise of the package resulting in a breach of the sterile barrier
May 18, 2016Medical DevicesFDA
Medtronic recalls Covidien Kangaroo Connect Enteral Feeding Pump Item Number: 584400 (OUS) Intended to provide enteral nutrition to a
Hazard: Kangaroo Connect Feeding Pump Occlusion alarms fail to alarm
May 18, 2016Medical DevicesFDA
Medtronic recalls Covidien Kangaroo Connect Enteral Feeding Pump Item Number: 384400 (US) Intended to provide enteral nutrition to a p
Hazard: Kangaroo Connect Feeding Pump Occlusion alarms fail to alarm
May 18, 2016Medical DevicesFDA
Medtronic recalls Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient Monitor, Battery Packs Model Number - 016400, 0105
Hazard: Medtronic Respiratory & Monitoring Solutions Announces a Voluntary Recall of a Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient Monitor Due to the Battery Pack Might Experience Thermal Runaway with the Potential of Fire Risk to the Monitor.