Medtronic, Inc. recalls
3 recalls filed under Medtronic, Inc.. The most recent was published May 6, 2026.
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Class II · 6 months ago
Medtronic Sphere-9 Catheter recall: Ventricular fibrillation (VF) occurred during radiofrequency (RF) therapy
Ventricular fibrillation (VF) occurred during radiofrequency (RF) therapy with the Medtronic Sphere-9 catheter in patients who have a Biotronik…
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Class II · 9 months ago
Medtronic Inc Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090 recall: Stents may be impacted by a Nitinol anomaly which causes a reduced stent
Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force. Issue may…
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Class II · 11 months ago
Medtronic, Inc. Aurora EV-ICD and Clinical EV-ICD, single chamber recall: There is a potential for delayed time to high-voltage (HV) therapy
There is a potential for delayed time to high-voltage (HV) therapy should a rare sequence of events occur.
About this page
Medtronic, Inc. appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.