Cerenovus, Inc.
465 devices · 3,094 adverse event reports · 20 deaths reported · 194 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- CEREPAK HELIFORM SHD100250DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100258DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100308DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100310DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100408Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD100410DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100510Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD100515Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD100612Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD100616Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD100716Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD100720DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100820Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD100925DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD180625DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD180733DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD180835Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD180935Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD181040DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD181242DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD181650Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD181855Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD182060DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD182260Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD182460DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM XCR120201Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM XHD100151Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM XHD100152DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100153DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100201Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM XHD100202Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM XHD100203DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100204Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM XHD100206DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100254DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100256Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM XHD100304Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM XHD100306Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM XHD100406DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM XHD100408DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX100305Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX100253Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX100202DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX100611Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX100816DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX100829Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX141016DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX141025DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX141118DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK Uniform FCX141127Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK Uniform FCX141219DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK Uniform FCX141230Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX140225DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140303DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140304DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140306Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX140445DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140406DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140408Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX140512DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140507Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX140615DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140609DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140711DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140717Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX140812Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX140820DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX140914Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX140922DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX181034Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX181137DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX181220DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX181240Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX181343DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX181550Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX181647Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX181750Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX181950DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX180612Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX180813DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX180830Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK UNIFORM FCX180915DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK UNIFORM FCX180933DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CODMAN 80-1396NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1397NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1398NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1400NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1401NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1402NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1404NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1406NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1409NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1449NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1450NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1451NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1452NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1453NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1454NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1455NEUROSURGICAL PADDIE1 recall0 reports
- CODMAN 80-1456NEUROSURGICAL PADDIE1 recall0 reports