7 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CONTAK RENEWAL 3
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code NIK·November 11, 2008
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·August 11, 2011
CONTINUOUS AUTO TRANSFUSION SYSTEM
FDA Adverse Event
Death
·FRESENIUS-KABI·Product code CAC·July 26, 2013
LASER PROBES
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER·Product code HQE·February 20, 2018
LASER PROBES
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER·Product code HQE·April 18, 2018
COLORECTAL CANCER SCREENING (IFOB) TEST KIT
FDA Adverse Event
Injury
·2SAN LLC.·Product code KHE·March 24, 2025
LASER PROBES
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER·Product code HQE·April 21, 2017