115 results
·
54ms
·
Sources: EU EUDAMED, US FDA
OHIO MEDICAL PRODUCTS
FDA Adverse Event
Injury
·OHIO MEDICAL PRODUCTS·Product code BTI·February 28, 2013
AMVEX FLOWMETER
FDA Adverse Event
Death
·OHIO MEDICAL LLC·Product code CAX·February 21, 2021
OHIO MEDICAL
FDA Adverse Event
Malfunction
·Product code KFZ·May 20, 2021
OHIO MEDICAL TWIN FLOWMETER
FDA Adverse Event
Malfunction
·OHIO MEDICAL LLC·Product code CAX·February 9, 2022
OHMEDA
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code CAX·November 9, 2011
DISS VACUUM LATCH VALVE
FDA Adverse Event
Other
·OHIO MEDICAL CORPORATION·Product code BTA·December 13, 2010
OHMEDA 1251 CONTINUOUS/INTERMITTENT VACUUM REGULATOR
FDA Adverse Event
Malfunction
·OHIO MEDICAL PRODUCTS·Product code KDP·October 21, 2019
7800 VENTILATOR
FDA Adverse Event
Malfunction
·OHIO MEDICAL PRODUCTS·Product code CBK·February 4, 1993
INTERMITTENT SUCTION REGULATOR
FDA Adverse Event
Malfunction
·OHIO MEDICAL CORPORATION·Product code KDP·May 7, 2007
OHIO MEDICAL
FDA Adverse Event
Other
·OHIO MEDICAL CORPORATION·Product code KDP·June 1, 2009
AMVEX OXYGEN FLOWMETER
FDA Adverse Event
Death
·OHIO MEDICAL LLC·Product code CAX·February 9, 2018
SMART PORT CT
FDA Adverse Event
Injury
·ANGIODYNAMICS, INC.·Product code LJT·May 20, 2026
AMVEX
FDA Adverse Event
Malfunction
·OHIO MEDICAL LLC·Product code CAX·April 23, 2025
MEDICAL GAS FLOWMETER
FDA Adverse Event
Injury
·OHIO MEDICAL LLC·Product code CAX·August 24, 2023
PUMP, INFUSION, IMPLANTED, PROGRAMMABLE
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·March 9, 2015
MEDEX CLEAR CUFF PRESSURE INFUSION
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code KZD·December 26, 2024
OHIO TRANSPORT INCUBATOR
FDA Adverse Event
Malfunction
·OHIO MEDICAL PRODUCT OHMEDA CO.·Product code FPL·June 26, 1998
MEDEX C FUSOR 500ML PRESSURE INFUSOR
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code KZD·November 20, 2024
OHIO MEDICAL COLLECTION BOTTLE
FDA Adverse Event
Malfunction
·OHIO MEDICAL LLC·Product code KDQ·September 14, 2017
OMI 7300 OPERATING TABLE
FDA Adverse Event
Other
·OHIO MEDICAL INSTRUMENT CO., INC.·Product code GDC·April 21, 2003