16 results
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35ms
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Sources: EU EUDAMED, US FDA
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FDA Adverse Event
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HEYER-SCHULTE SALINE-FILLED MAMMARY PROSTHESIS, 275 CC
FDA Adverse Event
V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FWM·November 15, 1994
AVENIR MLLER, STEM, STANDARD, UNCEMENTED, HA, 4, TAPER 12/14
FDA Adverse Event
Injury
·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LZO·August 13, 2021
GEMSTAR PAIN MGE SNG
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·August 30, 2013
FREESTYLE LITE
FDA Adverse Event
Malfunction
·Product code NBW·November 20, 2010
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORP.·Product code DSQ·March 12, 2013
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·February 7, 2011
PRECISION XTRA/OPTIUM
FDA Adverse Event
Injury
·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·February 26, 2008
VERSA-DIAL 46X24X47 HUM HEAD
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·April 24, 2013
PC HYBRID GLENOID POST- POLY
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·February 28, 2013
SM HYBRID GLENOID BASE 4MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·February 28, 2013
2.4MM SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW 2.7 X 10MM
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HWC·August 31, 2020
OXF UNI TIB TRAY SZ C RM PMA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·September 4, 2020
OXF ANAT BRG RT MD SIZE 4 PMA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·September 4, 2020
TMJ SYSTEM LEFT FOSSA COMPONENT, SMALL
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code LZD·August 31, 2020
TMJ SYSTEM LEFT STANDARD MANDIBULAR COMPONENT 50MM / 9 HOLE
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code LZD·August 31, 2020
PENUMBRA SMART COIL
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code HCG·August 31, 2022