272 results · 46ms · Sources: EU EUDAMED, US FDA

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PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code NEW·November 14, 2024

IMPELLA

FDA Adverse Event
Malfunction ·ABIOMED, INC. - 1220648·Product code OZD·February 27, 2026

ENDOWRIST

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 20, 2026

MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAN·January 23, 2024

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·January 23, 2024

HARMONIC SCALPEL 5MM HD SHEATH HOOK TIP

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 4, 2022

KIT, 14FR INTRODUCER, 13CM&25CM, STERILE

FDA Adverse Event
Malfunction ·ABIOMED, INC. - 1220648·Product code DYB·March 12, 2026

DAVINCI XI

FDA Adverse Event
Injury ·INTUITIVE SURGICAL, INC·Product code NAY·October 15, 2022

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·January 11, 2022

GORE DUALMESH® PLUS BIOMATERIAL

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code FTL·October 22, 2019

POD COIL

FDA Adverse Event
Malfunction ·PENUMBRA·Product code HCG·May 9, 2018

DAVINCI XI

FDA Adverse Event
Injury ·INTUITIVE SURGICAL, INC·Product code NAY·August 22, 2024

COOK CELECT NAVALIGN JUGULAR & FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·February 22, 2012

EMBLEM S-ICD

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·April 6, 2022

UNKNOWN VLOC PRODUCT

FDA Adverse Event
Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·March 10, 2023

GORE DUALMESH BIOMATERIAL

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code FTL·July 16, 2019

IMPELLA

FDA Adverse Event
Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 5, 2026

CORTRAK 2 ENTERAL ACCESS SYSTEM

FDA Adverse Event
Injury ·AVANOS MEDICAL INC.·Product code KNT·March 18, 2021

KIT, 14FR INTRODUCER, 13CM&25CM, STERILE

FDA Adverse Event
Malfunction ·ABIOMED, INC.·Product code DYB·March 8, 2026

PRESSURE SENTINEL FLEXIBLE REAMER

FDA Adverse Event
Malfunction ·ZIMMER, INC.·Product code HWE·May 31, 2012