665 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VITEK® 2 GRAM-POSITIVE ANTIMICROBIAL SUSCEPTIBILITY TEST AST-P632 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code LON·February 23, 2018
VITEK® 2 AST-P632 TEST CARD,
FDA Adverse Event
Malfunction
·BIOMERIEUX INC.·Product code LON·November 15, 2017
VITEK® 2 AST-P632 TEST CARD,
FDA Adverse Event
Malfunction
·BIOMERIEUX INC.·Product code LON·November 15, 2017
VITEK® 2 AST-P633 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code LON·June 28, 2018
VITEK® 2 GRAM-POSITIVE ANTIMICROBIAL SUSCEPTIBILITY TEST AST-P648 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code LON·March 14, 2018
VITEK® 2 GRAM-POSITIVE ANTIMICROBIAL SUSCEPTIBILITY TEST AST-P632 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code LON·March 21, 2018
COOK AIRWAY EXCHANGE CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code DQY·June 27, 2016
VITEK® 2 GRAM-POSITIVE ANTIMICROBIAL SUSCEPTIBILITY TEST AST-P654 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code LON·March 21, 2018
Liofilchem MTS (MIC Test Strip)
FDA UDI
LIOFILCHEM SRL·18055182873309·
LO-PRO TRACHEAL TUBE CUFFED, MURPHY EYE
FDA Adverse Event
Injury
·MALLINCKRODT INC.·Product code LNZ·February 4, 1994
TUBE, ENDOTRACHEAL
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code LNZ·November 26, 2018
ENDOTRACHEAL TUBE (8 SIZE)
FDA Adverse Event
Injury
·MALLINCKRODT·Product code LNZ·May 17, 1993
PORTEX CUFF INFLATOR PRESSURE GAUGE
FDA Adverse Event
Malfunction
·NULL·Product code LNZ·April 5, 2022
CURAPLEX
FDA Adverse Event
Malfunction
·MEDSOURCE LABS LLC·Product code LNZ·July 24, 2025
CURAPLEX
FDA Adverse Event
Malfunction
·MEDSOURCE LABS LLC·Product code LNZ·August 13, 2025
PORTEX CUFF PRESSURE MONITORING
FDA Adverse Event
Malfunction
·ST PAUL·Product code LNZ·November 23, 2021
CURAPLEX
FDA Adverse Event
Malfunction
·MEDSOURCE LABS LLC.·Product code LNZ·July 18, 2025
TRACHEAL TUBE
FDA Adverse Event
Malfunction
·Product code LNZ·October 19, 2021
TRACHEAL TUBE
FDA Adverse Event
Malfunction
·Product code LNZ·August 20, 2021
COVIDIEN
FDA Adverse Event
Malfunction
·MEDTRONIC INC.·Product code LNZ·March 31, 2023