Karl Storz SE & Co. Kg
FDA adverse event reports naming Karl Storz SE & Co. Kg as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: KARL STORZ SE & CO. KG.
- Total reports
- 5,916
- Deaths
- 42
- Injuries
- 1,771
- Malfunctions
- 4,100
Reports per year
617
4918
10319
14320
7821
19722
74223
66224
2,39425
1,54226
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Laryngoscope, RigidCCW1,009
- Laparoscope, General & Plastic SurgeryGCJ852
- Hysteroscope (And Accessories)HIH556
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI503
- Electrode, Electrosurgical, Active, UrologicalFAS476
- Endoscopic Video Imaging System/Component, Gastroenterology-UrologyFET408
- Insufflator, Automatic Carbon-Dioxide For EndoscopeFCX319
- Ureteroscope And Accessories, Flexible/RigidFGB202
- Confocal Optical ImagingOWN182
- Cystoscope And Accessories, Flexible/RigidFAJ164
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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