12 results
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46ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
K032008
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LJT·May 31, 2007
COMPRESSION SLEEVE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HSB·June 19, 2024
130° RADIOLUCENT TARGETING ARM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HSB·August 12, 2024
PENTA
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 26, 2013
FLO-GARD IV SOLUTION ADMIN SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MALTA·Product code FPA·March 28, 2011
LIFESHIELD NV PRIMARY PIGGYBACK SET
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·April 21, 2008
DLP SILICONE RCSP RETROGRADE RETROGRADE RETROGRADE CANNULA
FDA Adverse Event
Injury
·PERFUSION SYSTEMS·Product code DWF·December 9, 2020
COMPRESSION SLEEVE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HSB·May 14, 2025
GALILEO® LOCKING TOOL
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HSB·May 14, 2025
GALILEO® LOCKING TOOL
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HSB·May 14, 2025
COMPRESSION SLEEVE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HSB·May 14, 2025
BIOLOX DELTA, CERAMIC FEMORAL HEAD, L, 36/+3.5, TAPER 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·January 16, 2018