16 results · 19ms · 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.

VERSAPOINT

FDA Adverse Event
Malfunction ·ETHICON, INC.·Product code JOS·January 5, 2005

VERSAPOINT

FDA Adverse Event
Malfunction ·ETHICON, INC.·Product code JOS·January 5, 2005

VERSAPOINT

FDA Adverse Event
Malfunction ·ETHICON, INC.·Product code JOS·January 5, 2005

VERSAPOINT

FDA Adverse Event
Malfunction ·ETHICON, INC.·Product code JOS·January 5, 2005

VERSAPOINT

FDA Adverse Event
Malfunction ·ETHICON, INC.·Product code JOS·January 5, 2005

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 28, 2023

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·August 29, 2019

INTREL 3

FDA Adverse Event
Malfunction ·MDT PUERTO RICO OPERATIONS CO., MED REL·Product code LGW·August 2, 2011

SURESTEP

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CGA·September 10, 1999

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 24, 2016

ALARIS SYSTEM

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·April 22, 2022

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

INFUSOR

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 17, 2011

ARCHITECT C8000 SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·March 28, 2019

COBAS INTEGRA 400 PLUS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JGS·April 28, 2010

FASTTAKE

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CFR·June 6, 2003