2,507 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACCUVEIN HF470
FDA Adverse Event
Malfunction
·ACCUVEIN INC.·Product code KZA·December 14, 2016
ACCUVEIN
FDA Adverse Event
Malfunction
·ACCUVEIN INC.·Product code KZA·October 16, 2017
ACCUVEIN AV500
FDA Adverse Event
Malfunction
·ACCUVEIN INC.·Product code KZA·April 27, 2022
ACCUVEIN VEIN VISUALIZATION SYSTEM
FDA Adverse Event
Malfunction
·ACCUVEIN INC.·Product code KZA·September 3, 2024
ACCUVEIN VEIN VISUALIZATION SYSTEM
FDA Adverse Event
Malfunction
·ACCUVEIN, INC.·Product code KZA·January 10, 2023
VAIN FINDER
FDA Adverse Event
Malfunction
·ACCUVEIN LLC INC.·Product code KZA·September 27, 2023
ACCUVEIN AV400
FDA Adverse Event
Malfunction
·ACCUVEIN INC.·Product code KZA·September 15, 2020
ACCUVEIN POWERED WHEELED STAND
FDA Adverse Event
Malfunction
·ACCUVEIN INC.·Product code KZA·April 1, 2024
VEINVIEWER
FDA Adverse Event
CHRISTIE MEDICAL·Product code KZA·March 14, 2011
ACCUVEIN VEIN VISUALIZATION SYSTEM POWERED WHEELED STAND
FDA Adverse Event
Malfunction
·ACCUVEIN INC.·Product code KZA·July 16, 2024
ACCUVEIN
FDA Adverse Event
Malfunction
·ACCUVEIN, INC.·Product code KZA·March 8, 2017
ACCUVEIN AV500 AND ACCUVEIN HOLDER WITH POWER
FDA Adverse Event
Malfunction
·ACCUVEIN INC.·Product code KZA·April 14, 2026
AV400
FDA Adverse Event
Malfunction
·ACCUVEIN, INC.·Product code KZA·July 24, 2018
ACCUVEIN
FDA Adverse Event
Malfunction
·ACCUVEIN INC·Product code KZA·August 29, 2018
ACCUVEIN AV500 VEIN VISUALIZATION SYSTEM
FDA Adverse Event
Malfunction
·ACCUVEIN, INC.·Product code KZA·November 17, 2023
ACCUVEIN AV500 AND ACCUVEIN HOLDER WITH POWER
FDA Adverse Event
Malfunction
·ACCUVEIN INC.·Product code KZA·April 14, 2026
ACCUVEIN AV500 VEIN VISUALIZATION SYSTEM
FDA Adverse Event
Malfunction
·ACCUVEIN, INC.·Product code KZA·November 17, 2023
ACCUVEIN
FDA Adverse Event
Malfunction
·ACCUVEIN·Product code KZA·January 30, 2018
ACCU VEIN
FDA Adverse Event
Malfunction
·ACCUVEIN INC.·Product code KZA·November 27, 2019
VeinViewer (R) by Luminetx, Model Number VV1.0, Part No: P00399-L, Luminetx Corporation, Memphis, TN 38104 Product Usage: Non- invasive electronic visual aid device designed to project an image of a superficial subcutaneous vascular structures on the surface of the skin
FDA Recall
Terminated
·Christie Medical Holding Inc·Product code KZA·March 14, 2012