319 results · 50ms · Sources: EU EUDAMED, US FDA

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CAPSURE SP

FDA Adverse Event
Injury ·MPRI·Product code DTB·December 3, 2018

V3 RING UNIVERSAL

FDA Adverse Event
Injury ·DENTSPLY (N.Z.) LIMITED·Product code DZN·April 7, 2017

FLEXI-DAM

FDA Adverse Event
Injury ·DENT4YOU AG.·Product code EIE·September 19, 2024

MASTER PIN WITH THREAD

FDA Adverse Event
Injury ·HAGER & MEISINGER GMBH·Product code DZL·December 22, 2021

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·August 29, 2022

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·October 4, 2023

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 1, 2016

X-SMART PLUS VERSION 0202

FDA Adverse Event
Injury ·MAILLEFER INSTRUMENTS HOLDING SARL·Product code EGS·November 18, 2024

PERFIX PLUG

FDA Adverse Event
Injury ·DAVOL INC., SUB. C.R. BARD, INC. -1213643·Product code FTL·June 22, 2023

TRIATHLON CR X3 TIBIAL INSERT

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·June 15, 2021

UPSYLON Y MESH KIT

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code OHD·December 3, 2021

ELLIPS FX PHACO HANDPIECE

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code HQC·November 24, 2017

REMSTAR AUTO

FDA Adverse Event
Injury ·RESPIRONICS, INC.·Product code BZD·October 4, 2024

MENTOR MEMORYGEL BREAST IMPLANT

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code FTR·September 20, 2018

ARCTIC SUN® 5000

FDA Adverse Event
Injury ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·April 11, 2023

ANGIOSCULPT OTW PTA

FDA Adverse Event
Injury ·THE SPECTRANETICS CORPORATION·Product code PNO·September 30, 2022

Z NAIL CPM 11.5MM X 36CM 125 R

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code HSB·March 24, 2019

SET SCREW, 8 MM, 21 MM, HEX 3.5 MM

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code HSB·March 24, 2019

ACCOLADE TMZF HIP STEM #3

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·January 23, 2017

THERMOCOOL® SMARTTOUCH® BI-DIRECTIONAL NAVIGATION CATHETER

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·June 1, 2016