10,000 results
·
62ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
5FR POLY PQC
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD)·Product code LJS·July 24, 2006
TAMPAX TAMPON, VERSION/ABSORBENCY/SCENT UNKNOWN
FDA Adverse Event
Malfunction
·TAMBRANDS MANUFACTURING, INC·Product code HEB·November 18, 2025
BD ALARIS SMARTSITE
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS S.A DE C.V.·Product code LHI·June 30, 2025
DR. SCHOLL'S SKIN TAG REMOVER
FDA Adverse Event
SCHERING-PLOUGH HEALTHCARE PRODUCTS, INC.·Product code GEH·June 21, 2013
EVARREST FIBRIN SEALANT PATCH
FDA Adverse Event
Malfunction
·OMRIX BIOPHARMACEUTICALS LTD·Product code MZM·January 11, 2017
3 FR S/L PER-Q-CATH PLUS INTERMEDIATE TRAY
FDA Adverse Event
Injury
·C. R. BARD, INC. (BASD)·Product code LJS·March 31, 2011
4FR POLY PQC TRAY
FDA Adverse Event
Malfunction
·BARD REYNOSA S.A. DE C.V.·Product code LJS·July 21, 2003
4FR SL PQC PICC
FDA Adverse Event
Injury
·C.R. BARD, INC. (BASD)·Product code DQO·August 25, 2006
4FR POLY PQC TRAY
FDA Adverse Event
Injury
·BARD REYNOSA S.A. DE C.V.·Product code LJS·October 10, 2002
DR. BEST ZWISCHENZAHN MEDIUM
FDA Adverse Event
Injury
·Product code EFW·May 27, 2021
TAMPAXTAMPONSRADIANTRADIANTSUPERUNSCNT16CT
FDA Adverse Event
Malfunction
·TAMBRANDS MANUFACTURING, INC·Product code HEB·May 17, 2023
ALARIS SMARTSITE
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code LHI·February 27, 2025
DR. SCHOLL'S SKIN TAG REMOVER
FDA Adverse Event
Product code GEH·June 21, 2013
ALL-FLEX ARCHING SPRING DIAPHRAGM (SILICONE
FDA Adverse Event
Malfunction
·JOHNSON & JOHNSON MEDICAL BRAZIL·Product code HDW·March 24, 2014
TAMPAXTAMPONSRADIANTRADIANTFULLSIZEREGNORUNSCNT16CT
FDA Adverse Event
Malfunction
·TAMBRANDS MANUFACTURING, INC·Product code HEB·April 3, 2023
13 MM SS VIAL ACCESS DEVICE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code LHI·December 9, 2024
TAMPAXTAMPONSRADIANTRADIANTREGNORUNSCNT7CT
FDA Adverse Event
Malfunction
·TAMBRANDS MANUFACTURING, INC·Product code HEB·May 10, 2023
13 MM SS VIAL ACCESS DEVICE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code LHI·December 9, 2024
13 MM SS VIAL ACCESS DEVICE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code LHI·December 9, 2024
DR. SCHOLL'S FREEZE AWAY COMMON & PLANTAR WART REMOVER
FDA Adverse Event
Product code GEH·June 21, 2013