10,000 results
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1418ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NUTROPIN AQ PEN (SOMATROPIN) SOLUTION FOR INJECTION 10MG
FDA Adverse Event
GENENTECH, INC.·Product code KZE·March 10, 2010
NUTROPIN AQ PEN (SOMATROPIN) SOLUTION FOR INJECTION 10MG
FDA Adverse Event
GENENTECH, INC.·Product code KZE·February 17, 2010
NUTROPIN AQ PEN (SOMATROPIN) SOLUTION FOR INJECTION 10MG
FDA Adverse Event
GENENTECH, INC.·Product code KZE·May 21, 2010
NUTROPIN AQ PEN (SOMATROPIN) SOLUTION FOR INJECTION 10MG
FDA Adverse Event
Malfunction
·GENENTECH, INC.·Product code KZE·June 4, 2010
NOVO NORDISK AUTO COVER NEEDLES
FDA Adverse Event
Malfunction
·NOVO NORDISK·Product code KZE·April 1, 2010
CARPUJECT
FDA Adverse Event
Injury
·WINTHROP PHARMACEUTICALS·Product code KZE·July 3, 1996
NOVOLINPEN
FDA Adverse Event
NOVO NORDISK A/S·Product code KZE·September 4, 1996
MEDI-JECTOR
FDA Adverse Event
Injury
·MEDI-JECT CORP.·Product code KZE·August 7, 1996
NOVOPEN 1.5
FDA Adverse Event
Other
·NOVO NORDISK A/S·Product code KZE·September 30, 1996
HUMAPEN ERGO, TEAL/OPAQUE
FDA Adverse Event
Malfunction
·ELI LILLY AND CO.·Product code KZE·January 9, 2004
ACTIVA
FDA Adverse Event
Malfunction
·ACTIVA·Product code KZE·February 2, 2004
HUMAPEN ERGO, BURG/OPAQUE
FDA Adverse Event
Injury
·ELI LILLY AND CO.·Product code KZE·January 9, 2004
V-GO DISPOSABLE INSULIN DELIVERY DEVICE
FDA Adverse Event
Injury
·VALERITAS, LLC·Product code KZE·April 9, 2014
V-GO DISPOSABLE INSULIN DELIVERY DEVICE
FDA Adverse Event
Injury
·VALERITAS, INC·Product code KZE·October 23, 2014
J-TIP NEEDLE FREE INJECTION SYSTEM . 2ML
FDA Adverse Event
Injury
·NATIONAL MEDICLA PRODUCTS, INC.·Product code KZE·May 16, 2012
REBIJECT II
FDA Adverse Event
Malfunction
·EMD SERONO·Product code KZE·June 10, 2012
J-TIP NEEDLE FREE INJECTOR
FDA Adverse Event
Injury
·NATIONAL MEDICAL PRODUCTS, INC.·Product code KZE·April 24, 2012
HUMAPEN ERGO, BURG/CLEAR
FDA Adverse Event
Other
·ELI LILLY AND CO.·Product code KZE·March 28, 2002
HUMAPEN ERGO, TEAL/OPAQUE
FDA Adverse Event
Injury
·ELI LILLY AND CO.·Product code KZE·March 21, 2002
HUMAPEN ERGO, TEAL/OPAQUE
FDA Adverse Event
Malfunction
·ELI LILLY AND CO.·Product code KZE·March 28, 2002