19 results · 24ms · Sources: EU EUDAMED, US FDA

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COBAS AMPLIPREP / COBAS AMPLICOR HCV TEST, V2.0 CE-IVD

FDA Adverse Event
ROCHE MOLECULAR SYSTEMS·Product code MZP·December 19, 2012

COBAS AMPLIPREP / COBAS AMPLICOR HCV TEST, V2.0 CE-IVD

FDA Adverse Event
ROCHE MOLECULAR SYSTEMS·Product code MZP·December 19, 2012

RESTORE ULTRA

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·July 11, 2011

RESTORE ULTRA

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LGW·January 5, 2012

CANNULA, EGRESS, 3.0MM

FDA Adverse Event
Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code HRX·January 4, 2013

VASOVIEW HEMOPRO 2

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·March 8, 2013

MEDFUSION 3500 SYRINGE INFUSION PUMP

FDA Adverse Event
Malfunction ·SMITHS MEDICAL MD·Product code FRN·February 17, 2011

*

FDA Adverse Event
Malfunction ·*·Product code KDI·December 19, 2007

CANNULA, EGRESS, 3.0MM

FDA Adverse Event
Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code HRX·January 4, 2013

HEARTMATE 3 SYSTEM CONTROLLER

FDA Adverse Event
Malfunction ·THORATEC CORPORATION·Product code DSQ·May 22, 2023

CANNULA, EGRESS, 3.0MM

FDA Adverse Event
Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code HRX·June 11, 2012

PRIMEADVANCED

FDA Adverse Event
Malfunction ·IPG MFG SWITZERLAND·Product code LGW·July 22, 2016

CANNULA, EGRESS, 3.0MM

FDA Adverse Event
Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code HRX·February 6, 2013

KIT SHORT STEM FLEX 2-1/4

FDA Adverse Event
Malfunction ·COOPERSURGICAL, INC.·Product code HHW·February 22, 2021

RUMI II KOH-EFFICIENT

FDA Adverse Event
Injury ·COOPERSURGICAL, INC.·Product code HEW·August 7, 2024

SURESCAN

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·September 12, 2018

ACUVUE® VITA¿ FOR ASTIGMATISM

FDA Adverse Event
Injury ·JOHNSON & JOHNSON VISION CARE, INC. - US·Product code LPL·February 5, 2025

OASIS

FDA Adverse Event
Malfunction ·ATRIUM MEDICAL CORPORATION·Product code KDQ·February 3, 2025

OASIS

FDA Adverse Event
Malfunction ·ATRIUM MEDICAL CORPORATION·Product code KDQ·February 3, 2025