108 results
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60ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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THREADED CANNULA W/OBTURATOR (TRANSLUCENT, PURPLE)
FDA Adverse Event
Malfunction
·RENOVO, INC.·Product code NLM·April 5, 2021
THREADED CANNULA W/OBTURATOR (TRANSLUCENT, PURPLE)
FDA Adverse Event
Malfunction
·RENOVO, INC.·Product code NLM·April 5, 2021
ARTHROSCOPIC SHAVER, TORPEDO REGULAR LENGTH LIME GREEN
FDA Adverse Event
Malfunction
·RENOVO, INC.·Product code NLM·April 5, 2021
THREADED CANNULA W/OBTURATOR (TRANSLUCENT, PURPLE)
FDA Adverse Event
Malfunction
·RENOVO, INC.·Product code NLM·April 5, 2021
DYONICS ACROMIOBLASTER
FDA Adverse Event
Injury
·RENOVO, INC.·Product code HRX·May 19, 2026
DENOVO SPACE MAINTAINER BAND CHAIRSIDE SPACE MAINTAINER
FDA Adverse Event
Injury
·DENOVO DENTAL, INC.·Product code ECM·September 1, 2022
S 150 STAND-ALONE ANTERIOR CERVICAL INTERBODY FUSION
FDA Adverse Event
Malfunction
·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code OVE·March 22, 2017
TESERA 3-D PRINTED ALIF CAGE
FDA Adverse Event
Injury
·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code MAX·July 3, 2018
A200 KNEE SYSTEM
FDA Adverse Event
Injury
·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code JWH·September 16, 2016
A200 KNEE SYSTEM
FDA Adverse Event
Injury
·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code JWH·September 16, 2016
S100
FDA Adverse Event
Malfunction
·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code KWP·April 12, 2017
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·November 7, 2024
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·May 11, 2021
SHOCKWAVE IVL SYSTEM WITH THE SHOCKWAVE C2+ CORONARY IVL CATHETER
FDA Adverse Event
Malfunction
·SHOCKWAVE MEDICAL, INC.·Product code QMG·April 1, 2026
ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAT·March 20, 2023
THERMOCOOL® SMART TOUCH¿ BI-DIRECTIONAL NAVIGATION CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·March 18, 2024
IMPELLA 5.5 WITH SMARTASSIST S2 SET, US
FDA Adverse Event
Malfunction
·ABIOMED, INC. - 1220648·Product code OZD·March 18, 2026
IMPELLA 5.5 WITH SMARTASSIST S2 SET, US
FDA Adverse Event
Injury
·ABIOMED, INC. - 1220648·Product code OZD·March 19, 2026
SHOCKWAVE IVL SYSTEM WITH THE SHOCKWAVE C2+ CORONARY IVL CATHETER
FDA Adverse Event
Injury
·SHOCKWAVE MEDICAL, INC.·Product code QMG·April 24, 2026
KIT, 14FR INTRODUCER, 13CM&25CM, STERILE
FDA Adverse Event
Injury
·ABIOMED, INC. - 1220648·Product code DYB·March 3, 2026