62 results · 93ms · Sources: EU EUDAMED, US FDA

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TRICON/GENESIS KNEE

FDA Adverse Event
Injury ·SMITH & NEPHEW INC. ORTHOPAEDICS DIV.·Product code HSH·October 30, 1997

MOD II UNICOMPARTMENTAL KNEE SYSTEM

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC., ORTHOPAEDICS DIV.·Product code HTG·September 25, 1998

MAXIM PRIMARY TIB. BEAR

FDA Adverse Event
Injury ·BIOMET, INC.·Product code HSH·January 8, 2001

SWEET TIP BIPOLAR LEAD

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS·Product code DXY·September 8, 1997

BIOMET

FDA Adverse Event
Injury ·BIOMET, INC.·Product code JDI·January 2, 1998

VENTAK P2

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS·Product code LWS·August 5, 1998

VENTAK AV

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS·Product code LWS·February 8, 1998

ENDOTAK DOWN-SIZED PLUS

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS·Product code LWS·November 7, 1997

VENTAK AV AUTOMATIC CARDIOVERTOR DEFIBRILLATOR

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS·Product code LWS·November 7, 1997

SOFTFORM FACIAL IMPLANT

FDA Adverse Event
Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·June 22, 1998

SKLAR INSTRUMENTS

FDA Adverse Event
Injury ·SKLAR INSTRUMENTS·Product code HDF·September 17, 1997

ABBOTT AXSYM SYSTEM

FDA Adverse Event
Other ·ABBOTT MANUFACTURING, INC.·Product code JJE·August 11, 1997

COATED VICRYL (POLYGLACTIN 910) SUTURE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code GAM·July 13, 2004

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017

NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Malfunction ·COCHLEAR LTD.·Product code MCM·August 14, 1997

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 23, 2014

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·April 8, 2024

SHILEY CUFFLESS TRACHEOSTOMY TUBE

FDA Adverse Event
Malfunction ·MALLINCKRODT MEDICAL, INC.·Product code BTO·January 26, 1998

7200 SERIES MICROPROCESSOR VENTILAT

FDA Adverse Event
Injury ·PURITAN BENNETT·Product code CBK·November 24, 1997

ANGIO-SEAL

FDA Adverse Event
Injury ·QUINTON INSTRUMENT CO.·Product code MGB·October 7, 1997