111 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
UNIVERSAL ALIGNMENT HANDLE
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·June 9, 2010
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·February 1, 2006
ELASTIMIDE FOLDABLE SILICONE POSTERIOR CHAMBER INTRAOCULAR L
FDA Adverse Event
Injury
·STAAR SURGICAL CO.·Product code HQL·November 3, 2005
1.9F ARGYLE SINGLE LUMEN PICC
FDA Adverse Event
TYCO/KENDALL HEALTHCARE·Product code LJS·November 28, 2005
SINGLE TRAY KIT
FDA Adverse Event
Injury
·ARROW INTERNATIONAL, INC.·Product code LJT·April 17, 2006
BAXTER
FDA Adverse Event
Other
·BAXTER HEALTHCARE·Product code MEA·March 29, 2007
28CM DIALYSIS CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC.(BASD)·Product code DQO·September 29, 2005
HIRES 90K
FDA Adverse Event
Malfunction
·ADVANCED BIONICS CORP.·Product code MCM·November 18, 2005
PTFE VASCULAR GRAFTS SOFT>=6MM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC WAYNE·Product code DSY·October 26, 2005
ULTRAMER FOLEY TRAY
FDA Adverse Event
KENMEX·Product code EZL·June 22, 2005
SALUTE FIXATION DEVICE
FDA Adverse Event
Malfunction
·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·July 18, 2007
ULTRAMER FOLEY TRAY
FDA Adverse Event
KENMEX·Product code EZL·June 22, 2005
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code NIQ·January 10, 2006
RENU WITH MOISTURELOC
FDA Adverse Event
Injury
·BAUSCH AND LOMB·Product code LPN·April 13, 2006
LASER - INDIGO OPTIMA LASER SYSTEM
FDA Adverse Event
Injury
·ETHICON, INC.·Product code HQF·April 11, 2006
GUIDANT VASOVIEW 5 DISSECTION TIP
FDA Adverse Event
Malfunction
·GUIDANT CARDIAC SURGERY·Product code GEI·June 30, 2005
NATURAL-KNEE II SYSTEM CONGRUENT TIBIAL INSERT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·April 15, 2005
INDIGO OPTIMA LASER SYSTEM
FDA Adverse Event
Other
·ETHICON ENDO-SURGERY, INC. (CINCINNATI0·Product code GEX·November 17, 2005
NUCLEUS CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·October 28, 2005
GUIDANT
FDA Adverse Event
Death
·GUIDANT CORP·Product code DTB·March 17, 2008