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
- 5,708
- Deaths
- 42
- Injuries
- 1,723
- Malfunctions
- 3,940
Reports per year
617
4918
10319
14320
7821
19722
74223
66224
2,39425
1,33426
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Laryngoscope, RigidCCW945
- Laparoscope, General & Plastic SurgeryGCJ830
- Hysteroscope (And Accessories)HIH537
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI492
- Electrode, Electrosurgical, Active, UrologicalFAS467
- Endoscopic Video Imaging System/Component, Gastroenterology-UrologyFET390
- Insufflator, Automatic Carbon-Dioxide For EndoscopeFCX302
- Ureteroscope And Accessories, Flexible/RigidFGB198
- Confocal Optical ImagingOWN176
- Cystoscope And Accessories, Flexible/RigidFAJ157
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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