111 results · 27ms · Sources: EU EUDAMED, US FDA

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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