19 results
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24ms
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Sources: EU EUDAMED, US FDA
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FDA Adverse Event
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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