Medtronic Recalls
927 recalls on record in the United States
Medtronic Inc recalls 6F Taiga Guiding Catheter
Complaints regarding 6F Taiga guide catheter tip detachment and/or tip splitting.
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Medtronic Minimally Invasive Therapies Group recalls MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Cat
Medtronic is voluntarily recalling one lot of its MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays, Lot 1717900160, following notification from our supplier that one production lot of MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays was inadvertently shipped to Medtronic and distributed without being sterilized.
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Medtronic Minimally Invasive Therapies Group recalls Argyle Suction Tubing (Product # 8888301515) Argyle Suct
Incorrect packaging. In one lot of Argyle Suction Tubing, the pouch may be incorrectly labeled as the Salem Sump Dual Lumen Stomach Tube. This product may have been distributed within the case of Argyle Suction Tubing.
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Medtronic Neuromodulation recalls Medtronic Synchromed II Model 8637 supplied in 20mL and 40 m
Medtronic implemented a final design change intended to address the motor stall due to corrosion and is recalling devices with the previous design that are not implanted.
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Medtronic Navigation, Inc.-Littleton recalls O-arm 1000 mobile image-intensified fluoroscopic x-ray syste
Software update ("SW Update 3.2.1") is being implemented to address the following issues: Inability to power the system after shutdown, System stays in standalone mode, Image reconstruction, System/Pendant bootup, Dose display/report, Gantry motion, Network communication, System shutdown, and Early termination of 3D spin.
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Medtronic Perfusion Systems recalls BIO CAL(R) Temperature Controller, Models: (a) 370, (b) 370I
Medtronic has been unable to develop a cleaning protocol to satisfy current industry concerns and expectations. As a result, an updated cleaning protocol will not be developed by Medtronic and it has been determined that the best course of action is to request BIO CAL users to discontinue use and dispose of BIO CAL devices.
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Medtronic Navigation, Inc.-Littleton recalls O-arm¿ O2 interventional fluoroscopic x-ray system; Catalog
During servicing of certain internal components of the O-Arm O2 Surgical Imaging System, it is possible that the high-power cable connector may come in contact with surrounding metal during the disconnecting/reconnecting process which may result in an electrical short and a shock to the field service technician.
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Medtronic Perfusion Systems recalls Medtronic AFFINITY NT, Cardiotomy/Venous Reservoir (CVR) wit
Possible sterile barrier breach in the pouch of Affinity NT Cardiotomy Venous Reservoir stand alone uncoated and Affinity NT Cardiotomy Venous Reservoir stand alone Trillium coated products.
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Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Implantable Cardioverter Defibrillators (ICDs), Evera MRI.
Possible prevention of high and low voltage therapy in Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillator (CRT-D).
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Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Implantable Cardioverter Defibrillators (ICDs), Evera. Label
Possible prevention of high and low voltage therapy in Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillator (CRT-D).
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Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Implantable Cardioverter Defibrillators (ICDs), Visia AF. La
Possible prevention of high and low voltage therapy in Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillator (CRT-D).
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Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), V
Possible prevention of high and low voltage therapy in Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillator (CRT-D).
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Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Implantable Cardioverter Defibrillators (ICDs), Visia AF MRI
Possible prevention of high and low voltage therapy in Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillator (CRT-D).
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Medtronic Perfusion Systems recalls Medtronic TRILLIUM AFFINITY NT, Cardiotomy/Venous Reservoir
Possible sterile barrier breach in the pouch of Affinity NT Cardiotomy Venous Reservoir stand alone uncoated and Affinity NT Cardiotomy Venous Reservoir stand alone Trillium coated products.
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Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), C
Possible prevention of high and low voltage therapy in Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillator (CRT-D).
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Medtronic Inc. recalls Medtronic CareLink iPro Therapy Management Software, MMT-734
Due to a time conversion error, data uploaded from the iPro(TM)2 recorder to the CareLink iPro software using the new CareLink iPro Uploader feature may result in incorrect reports. This pertains only to reports generated between September 23, 2017 and September 27, 2017 that used the new CareLink iPro Uploader feature.
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Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), A
Possible prevention of high and low voltage therapy in Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillator (CRT-D).
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Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), C
Possible prevention of high and low voltage therapy in Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillator (CRT-D).
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Medtronic Sofamor Danek USA Inc recalls Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only
Medtronic has discovered the product lot in question was noted as having a longer drill tip extension than what is indicated on the print specification.
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Medtronic Neurosurgery recalls Model #: CG8900, Medtronic Clip Gun Scalp Clip Kit (Qty 1);
Medtronic is initiating a voluntary recall because the products identified above did not adequately demonstrate acceptable packaging performance to current standards.
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Medtronic Neuromodulation recalls Medtronic Ascenda(R) Intrathecal Catheter, Models: (a) 8780
There is a possibility that specific lots of catheters that have recently been distributed may be at risk for an increased potential for kinking at the proximal end where the catheter connects to the drug infusion pump.
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Medtronic Perfusion Systems recalls Medtronic Custom Perfusion Systems, indicated for use in the
Medtronic custom perfusion tubing packs contain Terumo OPS valves that were recalled due to a lack of flow through the valve.
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Medtronic Inc., Cardiac Rhythm and Heart Failure recalls MyCareLink Smart Patient Monitors. It is intended for use
Patients monitored on two (2) or more implanted Medtronic heart devices in the Medtronic CareLink Network may have potential impact on the ability to remotely monitor the patient's heart devices. Potential impacts could lead to missed CareAlert notifications or device reports.
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Medtronic Inc., Cardiac Rhythm and Heart Failure recalls MyCareLink Patient Monitors. It is intended for used with
Patients monitored on two (2) or more implanted Medtronic heart devices in the Medtronic CareLink Network may have potential impact on the ability to remotely monitor the patient's heart devices. Potential impacts could lead to missed CareAlert notifications or device reports.
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Medtronic Sofamor Danek USA Inc recalls Medtronic KYPHON(R) Express(TM) Directional Bone Filler Devi
Medtronic has discovered the directional arrow at the proximal end of the instrument may not correctly align with the cut out opening on the distal end of the instrument.
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Medtronic Inc. recalls Everflex Self-Expanding Peripheral Stent with Entrust Delive
Stent length on the label may not match the length of the stent itself.
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Medtronic Inc. recalls Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
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Medtronic Inc. recalls Medtronic MiniMed(TM) Sure-T(TM) (MMT-862, 862T, 864, 864T,
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
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Medtronic Inc. recalls Medtronic MiniMed(TM) Silhouette(TM) (MMT-377, 377T, 378, 37
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
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Medtronic Inc. recalls Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
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Showing 30 of 927 recalls. See all →