590 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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CADD LEGACY PUMP 1.5MG SDV
FDA Adverse Event
Injury
·SMITHS MEDICAL ASD, INC.·Product code FRN·September 26, 2018
GORE® DRYSEAL SHEATH
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code DYB·October 27, 2016
CATHETER
FDA Adverse Event
Injury
·UNKNOWN·Product code FOZ·October 8, 2024
IV ADMINISTRATION LINE
FDA Adverse Event
Injury
·UNKNOWN·Product code FPA·October 8, 2024
PROMUS PREMIER SELECT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·April 7, 2022
CADD PUMP SOLIS VIP
FDA Adverse Event
Injury
·ICU MEDICAL, INC./SMITHS MEDICAL·Product code FRN·November 12, 2025
SLIMPLICITY ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·SPINAL USA, INC·Product code KWQ·August 22, 2013
CADD EXTENSION SET
FDA Adverse Event
Injury
·SMITHS MEDICAL ASD, INC.·Product code FPA·February 3, 2023
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·February 13, 2013
SNOWDEN PENCER COTTLE
FDA Adverse Event
Injury
·BD V. MUELLER·Product code KAD·December 30, 2016
BD V. MUELLER
FDA Adverse Event
Injury
·BD-V. MUELLER / CAREFUSION 2200, INC.·Product code LXH·August 14, 2017
UNKNOWN CAGE/SPACER
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code ODV·June 8, 2021
UNKNOWN CAGE/SPACER
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code ODV·June 4, 2021
HICKMAN
FDA Adverse Event
Injury
·BARD·Product code MDV·March 14, 1994
BARD
FDA Adverse Event
Injury
·BARD ACCESS SYSTEMS·Product code MDV·January 25, 1994
UNKNOWN CAGE/SPACER
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code ODV·June 8, 2021
PORT-A-CATH EPIDURAL IMPLANTABLE ACCESS SYSTEM
FDA Adverse Event
Injury
·SMITHS MEDICAL MD (FORMELY DELTEC,INC).·Product code MDV·August 25, 2004
OMEGA PORT
FDA Adverse Event
Injury
·NORFOLK MEDICAL·Product code MDV·March 1, 1995
PORT-A-CATH EPIDURAL IMPLANTABLE ACCESS SYSTEM
FDA Adverse Event
Injury
·SIMS DELTEC, INC.·Product code MDV·October 27, 2000
OMEGA PORT
FDA Adverse Event
Injury
·NORFOLK MEDICAL PRODUCTS, INC.·Product code MDV·October 20, 1994