261 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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CARDIOXYL
FDA Adverse Event
Malfunction
·PETERS SURGICAL·Product code GAT·June 20, 2014
CARDIOXYL SUTURE
FDA Adverse Event
PETERS SURGICAL·Product code GAT·June 23, 2014
TLIFT®
FDA Adverse Event
Malfunction
·PETERS SURGICAL·Product code NWV·January 26, 2023
CARDIOXYL SUTURE
FDA Adverse Event
Injury
·PETERS SURGICAL·Product code GAT·March 19, 2014
T'LIFT
FDA Adverse Event
Malfunction
·PETERS SURGICAL·Product code NWV·February 22, 2023
VALIANT
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·October 9, 2014
PROSTHESIS, ELBOW, HEMI-, RADIAL
FDA Adverse Event
Injury
·ACUMED LLC·Product code KWI·April 8, 2019
EX-PRESS MINI GLAUCOMA SHUNT
FDA Adverse Event
Injury
·OPTONOL, LTD·Product code KYF·December 7, 2012
UNK_ULTRACISION HARMONIC FOCUS
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 27, 2019
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·June 29, 2015
STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·June 18, 2021
UNKNOWN VLOC PRODUCT
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·January 18, 2019
UNKNOWN PROTACK
FDA Adverse Event
Injury
·US SURGICAL PUERTO RICO·Product code GDW·January 18, 2019
KYPHX 11 GAUGE BONE ACCESS NEEDLE
FDA Adverse Event
Injury
·MEDTRONIC SPINE LLC·Product code HRX·March 11, 2009
UNKNOWN HIP FEMORAL STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·December 16, 2019
AORTIC EXCLUDER AAA ENDOPROSTHESIS (C3)
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·May 9, 2019
UNK_PATIENT RETURN ELECTRODES - REUSABLE
FDA Adverse Event
Injury
·MEGADYNE MEDICAL PRODUCTS, INC.·Product code GEI·October 8, 2019
SENTRANT INTRODUCER SHEATH
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code DYB·May 21, 2020
KYPHX HV-R BONE CEMENT
FDA Adverse Event
Injury
·MEDTRONIC SPINE LLC·Product code NDN·March 11, 2009
UNKNOWN COONRAD-MORREY HUMERAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JDC·February 15, 2017