1,032 results · 41ms · Sources: EU EUDAMED, US FDA

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ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·February 22, 2012

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·February 22, 2012

RESTORE RECHARGEABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·December 4, 2008

ULTRAPULSE ENCORE

FDA Adverse Event
Injury ·LUMENIS, LTD.·Product code GEX·September 16, 2011

ENDOPATH XCEL

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·July 29, 2013

PELVICOL ACELLULAR COLLAGEN MATRIX 4X7CM

FDA Adverse Event
Other ·UNITED STATES SURGICAL·Product code FTL·January 26, 2012

AMS INFLATABLE PENILE PROSTHESIS

FDA Adverse Event
Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FAE·October 31, 2013

6949 SPRINT FIDELIS

FDA Adverse Event
Malfunction ·MEDTRONIC·Product code NVY·August 12, 2023

SENSORMEDICS

FDA Adverse Event
Malfunction ·CAREFUSION·Product code LSZ·July 10, 2012

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM INC.·Product code MDS·March 31, 2014

DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIAL (RA) PACEMAKER ELE

FDA Adverse Event
Injury ·MEDTRONIC·Product code NVN·August 11, 2023

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM INC.·Product code MDS·March 31, 2014

BED, AC-POWERED ADJUSTABLE HOSPITAL

FDA Adverse Event
Malfunction ·UNKNOWN·Product code FNL·August 12, 2023

BED, AC-POWERED ADJUSTABLE HOSPITAL

FDA Adverse Event
Malfunction ·UNKNOWN·Product code FNL·August 12, 2023

BED, AC-POWERED ADJUSTABLE HOSPITAL

FDA Adverse Event
Malfunction ·UNKNOWN·Product code FNL·August 12, 2023

COVIDIEN ENDO GIA ULTRA UNIVERSAL STAPLER

FDA Adverse Event
Malfunction ·COVIDIEN·Product code GDW·July 25, 2012

B/F TRABECULAR METAL GLENOID DRILL W/STOP

FDA Adverse Event
Malfunction ·ZIMMER, INC.·Product code HSD·June 7, 2012

VISIAN ICL (IMPLANTABLE COLLAMER LENS)

FDA Adverse Event
Injury ·STAAR SURGICAL COMPANY·Product code MTA·January 15, 2013

IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT)

FDA Adverse Event
Malfunction ·MEDTRONIC·Product code LWS·August 11, 2023

2.4MM TI CORTEX SCREW SLF-TPNGWITH T8 STARDRIVE RECESS 12MM

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·May 3, 2013