7 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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BD Y SITE ASSEMBLY
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·June 26, 2023
ASSEMBLY NAC Y-SITE (0.104 POCKET) OEM
FDA Adverse Event
Malfunction
·Product code FPA·July 17, 2021
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 26, 2013
HC234 CPAP HUMIDIFIER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·May 24, 2011
COBAS 4800 HPV TEST
FDA Adverse Event
Malfunction
·ROCHE MOLECULAR SYSTEMS·Product code MAQ·July 17, 2017
THV 1000-29 3F AORTIC BIO 29MM
FDA Adverse Event
Malfunction
·MEDTRONIC 3F THERAPEUTICS, INC.·Product code LWR·December 5, 2025
THV 1000-29 3F AORTIC BIO 29MM
FDA Adverse Event
Malfunction
·MEDTRONIC HEART VALVES DIVISION·Product code LWR·December 17, 2024