10 results
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17ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
HEARTSTART FRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 28, 2013
CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNT·October 16, 2008
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 5, 2011
GMK SPHERE TOTAL KNEE SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code JWH·November 18, 2025
Cure Catheter® Closed System
FDA Adverse Event
Malfunction
·CONVATEC INC·Product code FCM·August 23, 2022
Cure Catheter® Closed System
FDA Adverse Event
Malfunction
·CONVATEC INC·Product code FCM·August 23, 2022
Cure Catheter® Closed System
FDA Adverse Event
Malfunction
·CONVATEC INC·Product code FCM·August 23, 2022
BD PHASEAL¿ IV BAG/LINE ACCESS DEVICES
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code ONB·November 9, 2022
GMK SPHERE TOTAL KNEE SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code JWH·April 15, 2026
GMK TOTAL KNEE SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code JWH·March 17, 2025