22 results · 37ms · Sources: EU EUDAMED, US FDA

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SYNTHES ANTERIOR CERVICAL PLATE

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code JDN·May 21, 1997

CAPTURE-R READY INDICATOR RED CELLS

FDA Adverse Event
Malfunction ·IMMUCOR·Product code KSZ·May 18, 2007

TRIMPORT IMPLANTABLE VASCULAR ACCESS SYSTEM

FDA Adverse Event
GERARD MEDICAL, INC.·Product code LJT·June 6, 1997

VENTAK MINI+ IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS·Product code LWS·March 6, 1997

ZYPLAST COLLAGEN IMPLANT

FDA Adverse Event
Injury ·COLLAGEN CORP.·Product code LMH·October 10, 1997

VENTAK MINI+ IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 16, 1997

SELECT SHOULDER COGR HUMERAL HEAD 52 X 26

FDA Adverse Event
Injury ·SULZER ORTHOPEDICS, INC.·Product code HSD·August 22, 1997

TRIMPORT IMPLANTABLE VASCULAR

FDA Adverse Event
Malfunction ·GERARD MEDICAL, INC.·Product code LJT·October 2, 1997

VALLEYLAB ELECTROSURGICAL GENERATOR

FDA Adverse Event
Malfunction ·VALLEYLAB, INC.·Product code GEI·July 24, 1998

CAPTURE-R READY-ID TEST WELLS

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·May 11, 2007

28MM COCR MOD HD +6MM NO SKIRT

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·January 30, 2015

EXTENSION TUBE, 10 CM LENGTH, 15F/15M

FDA Adverse Event
Malfunction ·MALLINCKRODT MEDICAL, INC SPA·Product code CAH·December 9, 1996

28MM MOD HD STD NECK TP1 TAPER

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·January 30, 2015

ULTRA-THIN BALLOON DILATATION CATHETER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC·Product code LIT·November 6, 2008

E SERIES DEFIBRILLATOR

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·August 17, 2011

SPECTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·July 5, 2013

3M FLUID RESISTANT FACE MASK

FDA Adverse Event
Injury ·3M MEDICAL PLANT·Product code FXX·August 6, 1997

PALMAZ SCHATZ BALLOON EXPANDABLE STENT WITH DELIVERY SYSTEM

FDA Adverse Event
Injury ·CORDIS, A JOHNSON AND JOHNSON CO·Product code MAF·April 15, 1998

BD INSULIN SYRINGES WITH BD ULTRA-FINE¿ NEEDLE

FDA Adverse Event
Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·June 28, 2023

IMPL TAPERED SCR-V SBM 6M M 5.7MM 10MM

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·July 19, 2019