12 results
·
49ms
·
Sources: EU EUDAMED, US FDA
SAFSITE®
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL INC.·Product code FPA·August 13, 2025
BD 2 PC 10ML DISCARDIT II SYRINGE W/O NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·February 10, 2020
UNKNOWN_NEUROVASCULAR_PRODUCT
FDA Adverse Event
Injury
·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code NRY·May 12, 2022
UNKNOWN OXFORD FEMORAL COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·August 22, 2025
UNKNOWN OXFORD FEMORAL COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·August 26, 2025
UNKNOWN OXFORD BEARING
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·August 22, 2025
UNKNOWN OXFORD BEARING
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·August 26, 2025
UNKNOWN OXFORD FEMORAL COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·August 22, 2025
UNKNOWN OXFORD BEARING
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·August 26, 2025
MOTIVA SILKSURFACE PLUS WITH QID
FDA Adverse Event
Injury
·ESTABLISHMENT LABS S.A.·Product code FTR·March 19, 2025
UNKNOWN OXFORD BEARING
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·October 1, 2025
ASP 6025 Vacuum Tissue Processor; an automated modular tissue processor; Leica Biosystems Nussloch GmbH, Heidelberger Str. 17-19, D-69226 Nussloch, Germany; The intended use of this device is as an automated system used to process tissue specimens for examination through fixation, dehydration, and infiltration.
FDA Recall
Terminated
·Leica Microsystems, Inc.·Product code IEO·March 30, 2012