Medtronic, Inc. recalls
6 recalls.
- CareLink SmartSync Device Manager App recall (Medtronic, Inc.)
Medical deviceClass IIReported November 4, 2026 · Software problem has the potential for an inaccurate displayed longevity estimate. - CareLink SmartSync recall (Medtronic, Inc.)
Medical deviceClass IIReported November 4, 2026 · Software problem has the potential for an inaccurate displayed longevity estimate. - CareLink SmartSync Programmer recall (Medtronic, Inc.)
Medical deviceClass IIReported November 4, 2026 · Software problem has the potential for an inaccurate displayed longevity estimate. - OmniaSecure Model 3930M recall (Medtronic, Inc.)
Medical deviceClass IIReported November 4, 2026 · Affected leads require additional engineering evaluation due to complaints regarding difficulty in achieving fixation during implantation. Potential harm of... - Medtronic Sphere-9 Catheter recall (Medtronic, Inc.)
Medical deviceClass IIReported May 6, 2026 · Ventricular fibrillation (VF) occurred during radiofrequency (RF) therapy with the Medtronic Sphere-9 catheter in patients who have a Biotronik Implantable... - Abre Venous Self-Expanding Stent System recall (Medtronic Inc)
Medical deviceClass IIReported January 21, 2026 · Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force. Issue may result in...