7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SUPERION INDIRECT DECOMPRESSION SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code NQO·June 20, 2023
SUPERION INDIRECT DECOMPRESSION SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code NQO·June 20, 2023
2.7MM TI VA LCKNG SCR SLF-TPNG WITH T8 STARDRIVE RECESS 12MM--STERILE
FDA Adverse Event
Malfunction
·SYNTHES SELZACH·Product code HRS·June 23, 2016
PREVALON AIR TURN AND POSITION SYSTEM
FDA Adverse Event
Injury
·SAGE PRODUCTS LLC·Product code FMR·October 9, 2014
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 8, 2014
PORTEX BLUE LINE ULTRA TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL LTD.·Product code BTO·October 12, 2012
REPLY
FDA Adverse Event
Malfunction
·SORIN BIOMEDICA CRM S.R.L.·Product code NVZ·August 10, 2010