10,000 results · 1418ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

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