11 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TUFF-TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 15, 2024
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·October 6, 2024
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·August 15, 2024
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·July 23, 2024
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·August 21, 2025
FEMUR CEMENTED CRUCIATE RETAINING (CR) NARROW LEFT SIZE 6
FDA Adverse Event
Malfunction
·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code MBH·January 11, 2023
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·March 12, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 11, 2014
RESTORE ULTRA
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 17, 2011
BONE CEMENT DOUGHTYPE RADIOPAQUE 40 G POLYMER POWDER
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL, INC.·Product code LOD·April 2, 2018
MENTOR SMOOTH ROUND HIGH PROFILE
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FWM·January 6, 2025