Medtronic Cryocath LP
FDA adverse event reports naming Medtronic Cryocath LP as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC CRYOCATH LP.
- Total reports
- 9,420
- Deaths
- 244
- Injuries
- 4,526
- Malfunctions
- 4,650
Reports per year
14712
21413
23514
47915
55416
71917
96218
86519
67720
59921
52022
57323
68424
1,24325
72926
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FibrillationOAE3,501
- Catheter, SteerableDRA3,321
- Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible ElectroporationQZI1,904
- Cardiac Ablation Percutaneous CatheterLPB396
- Catheter, Electrode Recording, Or Probe, Electrode RecordingDRF231
- CableISN24
- Introducer, CatheterDYB20
- Wire, Guide, CatheterDQX9
- Unit, Cryosurgical, AccessoriesGEH3
- Catheter, PercutaneousDQY2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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