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

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CADD LEGACY PUMP 1.5MG SDV

FDA Adverse Event
Injury ·SMITHS MEDICAL ASD, INC.·Product code FRN·September 26, 2018

GORE® DRYSEAL SHEATH

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code DYB·October 27, 2016

CATHETER

FDA Adverse Event
Injury ·UNKNOWN·Product code FOZ·October 8, 2024

IV ADMINISTRATION LINE

FDA Adverse Event
Injury ·UNKNOWN·Product code FPA·October 8, 2024

PROMUS PREMIER SELECT

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·April 7, 2022

CADD PUMP SOLIS VIP

FDA Adverse Event
Injury ·ICU MEDICAL, INC./SMITHS MEDICAL·Product code FRN·November 12, 2025

SLIMPLICITY ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·SPINAL USA, INC·Product code KWQ·August 22, 2013

CADD EXTENSION SET

FDA Adverse Event
Injury ·SMITHS MEDICAL ASD, INC.·Product code FPA·February 3, 2023

GORE EXCLUDER AAA ENDOPROSTHESIS

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code MIH·February 13, 2013

SNOWDEN PENCER COTTLE

FDA Adverse Event
Injury ·BD V. MUELLER·Product code KAD·December 30, 2016

BD V. MUELLER

FDA Adverse Event
Injury ·BD-V. MUELLER / CAREFUSION 2200, INC.·Product code LXH·August 14, 2017

UNKNOWN CAGE/SPACER

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL CH·Product code ODV·June 8, 2021

UNKNOWN CAGE/SPACER

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL CH·Product code ODV·June 4, 2021

HICKMAN

FDA Adverse Event
Injury ·BARD·Product code MDV·March 14, 1994

BARD

FDA Adverse Event
Injury ·BARD ACCESS SYSTEMS·Product code MDV·January 25, 1994

UNKNOWN CAGE/SPACER

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL CH·Product code ODV·June 8, 2021

PORT-A-CATH EPIDURAL IMPLANTABLE ACCESS SYSTEM

FDA Adverse Event
Injury ·SMITHS MEDICAL MD (FORMELY DELTEC,INC).·Product code MDV·August 25, 2004

OMEGA PORT

FDA Adverse Event
Injury ·NORFOLK MEDICAL·Product code MDV·March 1, 1995

PORT-A-CATH EPIDURAL IMPLANTABLE ACCESS SYSTEM

FDA Adverse Event
Injury ·SIMS DELTEC, INC.·Product code MDV·October 27, 2000

OMEGA PORT

FDA Adverse Event
Injury ·NORFOLK MEDICAL PRODUCTS, INC.·Product code MDV·October 20, 1994