10 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SURGICAL SIMPLEX CEMENT
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·May 5, 2010
SIMPLEX P-JAPANESE TWIN PACK
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·March 10, 2010
SIMPLEX P-JAPANESE TWIN PACK
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·August 16, 2010
LIFE SCOPE G9
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·March 18, 2025
LIFE SCOPE G9
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·March 18, 2025
LIFE SCOPE G9
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·March 18, 2025
CROSSFIRE 10 DEG INSERT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·March 10, 2015
MINIMED INFUSION PUMP
FDA Adverse Event
Malfunction
·MINIMED INC.·Product code LZG·August 29, 1997
MONARCH IOL DELIVERY SYSTEM - CARTRIDGE
FDA Adverse Event
Malfunction
·ALCON LABORATORIES, INC. / HUNTINGTON·Product code KYB·February 15, 2001
AUTO SUTURE ROTIC ENDO GRASP 5MM
FDA Adverse Event
Malfunction
·UNITED STATES SURGICAL CORPORATION·Product code GCJ·March 29, 1999