367 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Open, Classified
×
Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS
FDA Recall
Open, Classified
·Medtronic Navigation, Inc.·Product code OLO·November 28, 2023
Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS
FDA Recall
Open, Classified
·Medtronic Navigation, Inc.·Product code OLO·November 28, 2023
Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only
FDA Recall
Open, Classified
·Micro Therapeutics, Inc.·Product code KRA·June 30, 2022
Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only
FDA Recall
Open, Classified
·Micro Therapeutics, Inc.·Product code KRA·June 30, 2022
Stealth S8 Clinical Software Application, REF: 9735762, CE0344, Rx Only. Used in the StealthStation System as an aid for locating anatomical structures in either open or percutaneous neurosurgical procedures.
FDA Recall
Open, Classified
·Medtronic Navigation, Inc.·Product code HAW·March 26, 2024
MiniMed 640G, insulin pump, Ref/Model # MMT-1711K, MMT-1752K, MMT-1752, Rx Only - Product Usage: indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin.
FDA Recall
Open, Classified
·Medtronic Inc.·Product code N/A·April 30, 2020
Cobalt XT DR MRI SureScan, Model Number DDPA2D1, Implantable Cardioverter Defibrillator
FDA Recall
Open, Classified
·Medtronic Inc.·Product code LWS·April 16, 2024
VenaSeal Closure System
FDA Recall
Open, Classified
·Medtronic Inc.·Product code PJQ·March 23, 2021
Medtronic REF: MMT-7020C Guardian Sensor (3) kit for the following packaging: GS3 SEMI 5PK OUS/ GTIN: 20763000192086, 5PK SF NEW GS3 OUS/GTIN: 20763000358451 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes. *Product not distributed within US.
FDA Recall
Open, Classified
·Medtronic Inc.·Product code MDS·February 26, 2021
Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Cobalt Crome application, Software Model Number D00U005; 2. Claria Amplia Compia application, Software Model Number D00U009; 3. Evera MRI application, Software Model Number D00U010; 3. Visia AF application, Software Model Number D00U011; 5. Viva Brava Evera application, Software Model Number D00U012;
FDA Recall
Open, Classified
·Medtronic, Inc.·Product code NVZ·June 18, 2025
Medtronic SmartLink software loaded on CareLink SmartSync Device Manager, Model Number 24967A with the following software components: 1. Azure Astra application, Software Model Number D00U003; 2. Percepta Serena Solara application, Software Model Number D00U004; 3. Cobalt Crome application, Software Model Number D00U005; 4. Micra VR application, Software Model Number D00U006; 5. Micra AV application, Software Model Number D00U007; 6. Viva Consulta Syncra Advisa Ensura application, Software Model Number D00U008; 7. Claria Amplia Compia application, Software Model Number D00U009; 8. Evera MRI application, Software Model Number D00U010; 9. Visia AF application, Software Model Number D00U011; 10. Viva Brava Evera application, Software Model Number D00U012; 11. Micra VR2 AV2 application, Software Model Number D00U022.
FDA Recall
Open, Classified
·Medtronic, Inc.·Product code KRG·June 17, 2025
Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, cardiac ablation, for treatment of atrial flutter.
FDA Recall
Open, Classified
·Medtronic, Inc.·Product code OAD·March 11, 2026
Medtronic MiniMed 620G Insulin Infusion Pump, Ref #s/Model(s) - MMT-1510, MMT-1710, and MMT-1750 *Not Distributed within the US
FDA Recall
Open, Classified
·Medtronic Inc.·Product code OZP·November 21, 2019
Cobalt XT HF CDT-D MRI SureScan, Model Number: DTPA2D4, Implantable Cardioverter Defibrillator
FDA Recall
Open, Classified
·Medtronic Inc.·Product code NIK·April 16, 2024
MIRRO MRI VR SureScan, Model Number DVME3D4, Implantable Cardioverter Defibrillator
FDA Recall
Open, Classified
·Medtronic Inc.·Product code LWS·April 16, 2024
Medtronic, REF: MMT-7008A, Enlite Glucose Sensor for the following packaging: ENLITE PLUS 5PK 23L 1CL /GTIN: 20643169541706, ENLT PLUS 5PK 2L 1CL PR/ GTIN: 20643169786725, ENLITE PLUS 5PK 23L 1CL/ GTIN: 20763000421292 - Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes.
FDA Recall
Open, Classified
·Medtronic Inc.·Product code MDS·February 26, 2021
Medtronic REF: MMT-7020D4 Guardian Sensor (3) for the following packaging: GS3 1PK 2L CANADA/ GTIN: 00763000179595 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes. *Product not distributed within US.
FDA Recall
Open, Classified
·Medtronic Inc.·Product code MDS·February 26, 2021
Aurora EV-ICD and Clinical EV-ICD, single chamber, extravascular implantable cardioverter defibrillators (ICD), Product Number DVEA3E4
FDA Recall
Open, Classified
·Medtronic, Inc.·Product code LWS·October 29, 2025
Medtronic MiniMed(TM) Silhouette(TM) (MMT-377, 377T, 378, 378T, 384, 384T, 368, 368T, 381, 381T, 382, 382T, 383, 383T)
FDA Recall
Open, Classified
·Medtronic Inc.·Product code FPA·September 10, 2017
Medtronic REF: MMT-7020C4 Guardian Sensor (3) for the following packaging: GS3 5PK 2L CANADA/ GTIN: 20763000179612 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes. *Product not distributed within US.
FDA Recall
Open, Classified
·Medtronic Inc.·Product code MDS·February 26, 2021