13 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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ID NOW COVID-19 2.0 TEST KIT 24T (EUA)
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 7, 2023
ID NOW COVID-19 2.0 TEST KIT 24T (EUA)
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 22, 2023
ASSEMBLY NAC-Y SITE (0.088 TUBING) OEM
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·July 23, 2020
BD ASSEMBLY NAC-Y SITE
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·December 12, 2023
ASSEMBLY NAC-Y SITE (0.088 TUBING)
FDA Adverse Event
Malfunction
·Product code FPA·September 14, 2021
BD ASSEMBLY NAC-Y SITE (0.088 TUBING) OEM
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·February 10, 2025
ASSEMBLY NAC-Y SITE (0.088 TUBING) OEM
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·February 12, 2021
ASSEMBLY NAC-Y SITE (0.088 TUBING) OEM
FDA Adverse Event
Malfunction
·Product code FPA·August 16, 2021
UNSPECIFIED BD Y-SITE BLUE VALVE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FPA·June 30, 2020
BD ALARIS¿ ASSEMBLY NAC Y-SITE TUBING
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·July 8, 2022
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 26, 2013
DRIVE SHAFT-MINIMUM 360MM LENGTH-FOR USE WITH RIA
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HTO·September 18, 2014
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·May 13, 2011