876 results · 37ms · 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

R SERIES

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 21, 2025

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

C0R50, 12X130 KII BALLOON BLNT TIP 6/BX

FDA Adverse Event
Malfunction ·APPLIED MEDICAL RESOURCES·Product code GCJ·March 2, 2017

BD POSIFLUSH¿ XS PRE-FILLED FLUSH SYRINGE NACL 0.9%

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND CO.·Product code NGT·July 3, 2019

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

CB030, 5MMX35CM EPIX LAPA SCISSOR, 10/BX

FDA Adverse Event
Malfunction ·APPLIED MEDICAL RESOURCES·Product code HET·February 24, 2022

ALARIS PUMP MODULE SMARTSITE INFUSION SET

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·February 2, 2022

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

INNER SHEATH, FOR 26 FR. OUTER SHEATH

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·July 26, 2024

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

2008T HEMODIALYSIS SYS., WITH CDX

FDA Adverse Event
Malfunction ·CONCORD MANUFACTURING·Product code KDI·July 18, 2023