5 results
·
13ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
BIOMET AGC V2 INTERLOK TIBIAL 22X 67MM
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code HRY·June 16, 2017
AGC V2 INTERLOK TIB 10X 71MM
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code HRX·May 19, 2017
HEMOSPLIT, 14.5 FR ST 19CM STANDARD KIT
FDA Adverse Event
Malfunction
·BARD ACCESS SYSTEMS INC.·Product code MSD·May 28, 2014
POWER PRO AMBULANCE COT
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIVISION·Product code FPO·December 7, 2010
AGC REVISION KNEE TIBIAL AUGMENTATION
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code JWH·June 28, 2017