319 results
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50ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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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