16 results · 35ms · Sources: EU EUDAMED, US FDA

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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