60 results
·
68ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CARE E VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·January 27, 2010
CARE E VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·January 27, 2010
CARE E VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·January 27, 2010
CARE E VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·January 27, 2010
CARE E VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·May 3, 2010
CARE E VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·January 27, 2010
CARE E VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·January 27, 2010
CARE-E-VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·September 18, 2013
OHIO MEDICAL
FDA Adverse Event
Other
·OHIO MEDICAL CORPORATION·Product code KDP·June 1, 2009
NA
FDA Adverse Event
Malfunction
·BEMIS MFG COMPANY·Product code KDQ·January 27, 2014
INTERMITTENT SUCTION REGULATOR
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code KDP·May 7, 2007
CARE-E-VAC 3
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·December 13, 2013
CARE E VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·July 27, 2009
CARE E VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·July 27, 2009
CARE-E-VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·May 3, 2010
OXYGEN FLOWMETER
FDA Adverse Event
Injury
·OHIO MEDICAL CORPORATION·Product code CAX·July 27, 2011
CARE E VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·January 27, 2010
CARE E VAC III
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code BTA·January 27, 2010
OHIO MEDICAL NPWT WOUND CARE KIT
FDA Adverse Event
Other
·OHIO MEDICAL CORPORATION·Product code OMP·May 3, 2010
MOBLVAC WC
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code OMP·May 7, 2010