14 results
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66ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
ULTHERA SYSTEM
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC.·Product code OHV·May 6, 2021
ULTHERA SYSTEM
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC.·Product code OHV·November 18, 2021
ULTHERA SYSTEM
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC.·Product code OHV·September 8, 2025
PROLARYN PLUS INJECTABLE IMPLANT
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC.·Product code MIX·July 15, 2021
ULTHERA SYSTEM
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC.·Product code OHV·July 6, 2021
ULTHERAPY
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC.·Product code OHV·March 10, 2023
ULTHERA SYSTEM
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC.·Product code OHV·June 2, 2023
ULTHERA SYSTEM
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC.·Product code OHV·December 21, 2022
THE CELLFINA SYSTEM
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC.·Product code OUP·March 17, 2020
ULTHERA SYSTEM
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC.·Product code OHV·December 21, 2022
ULTHERAPY
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC.·Product code OHV·February 26, 2021
COAPTITE
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC.·Product code LNM·June 15, 2018
PROLARYN PLUS
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC (FRANKSVILLE)·Product code KHJ·September 4, 2025
PROLARYN GEL
FDA Adverse Event
Malfunction
·MERZ NORTH AMERICA, INC (FRANKSVILLE)·Product code LMH·June 26, 2025