18 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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SALINE INFLATABLE ROUND BREAST IMPLANT, 425 AND 25 CC
FDA Adverse Event
MENTOR CORP.·Product code FWM·December 21, 1993
PORTEX TRACHEAL TUBE CLEAR MURPHEY EYESOFT SEAL
FDA Adverse Event
Malfunction
·ICU MEDICAL HEALTHCARE MANUFACTURING S.A. DE C.V·Product code BTR·March 18, 2026
DT UNIVERSAL DRILL
FDA Adverse Event
Malfunction
·RECHERCHES TECHNIQUES DENTAIRES (R.T.D.)·Product code DZA·March 19, 2019
ARCHITECT I2000SR
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code JJE·January 11, 2023
CELL-DYN 1200 ANALYZER
FDA Adverse Event
Other
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·July 15, 2005
ELECTRIC SYSTEMS FOOT CONTROL
FDA Adverse Event
Malfunction
·THE ANSPACH EFFORT, INC.·Product code HBC·February 14, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·August 11, 2014
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·ANIMAS CORP.·Product code LZG·February 19, 2008
SMR GLENOSPHERE DIA.36MM
FDA Adverse Event
Malfunction
·LIMACORPORATE S.P.A.·Product code PHX·June 16, 2022
INTELLIS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·November 9, 2018
NUCLISENS® EASYMAG® MAGNETIC SILICA
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code PPM·August 16, 2022
NUCLISENS® EASYMAG® MAGNETIC SILICA
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code PPM·August 16, 2022
SMR GLENOSPHERE Ø 36MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A·Product code MBF·March 24, 2023
MOBILE LINER INT 28 MM 42 MM
FDA Adverse Event
Injury
·LIMACORPORATE SPA·Product code LZO·April 16, 2021
CELL-DYN 1800 ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·June 26, 2009
CD1800 ANALYZER
FDA Adverse Event
Other
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·August 20, 2007
SUR-FIT NATURA PC DURAHESIVE CONVEX WAFER
FDA Adverse Event
Injury
·CONVATEC INC.·Product code EXE·December 26, 2013
INTELLIS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·April 20, 2020