10 results
·
45ms
·
Sources: EU EUDAMED, US FDA
QUICKIE QM710
FDA Adverse Event
Injury
·SUNRISE MEDICAL (US) LLC·Product code ITI·April 3, 2018
etouchus, model no. ETM-G01. Noninvasive Blood glucose meter.
FDA Recall
Open, Classified
·Touch US Llc·Product code NBW·June 21, 2022
etouchus, model no. ETM-G01. Noninvasive Blood glucose meter.
FDA Enforcement
Class II
·Ongoing·Touch US Llc·August 3, 2022
MEERA EU WITHOUT AUTO DRIVE
FDA Adverse Event
Malfunction
·HOLGER ULLRICH·Product code FQO·February 22, 2019
DEKA SMARTXIDE2
FDA Adverse Event
Injury
·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·November 3, 2023
AquaC UNO H [120V, 60Hz, 1000VA, Fresenius US-Version: 24-10VA-1 Vivonic Part Number: G02000970-US
FDA Recall
Open, Classified
·Fresenius Medical Care Holdings, Inc.·Product code FIP·June 16, 2022
AquaC UNO H [120V, 60Hz, 1700VA, Fresenius US-Version: 24-0970-1 Vivonic Part Number: G02000966-US
FDA Recall
Open, Classified
·Fresenius Medical Care Holdings, Inc.·Product code FIP·June 16, 2022
DJO STIMULATOR
FDA Adverse Event
Injury
·DJO LLC·Product code LOF·March 22, 2013
ALPHAMAXX (460 MM LONGIT. SHIFT), EU
FDA Adverse Event
Malfunction
·HOLGER ULLRICH·Product code FQO·February 15, 2018
CAPNOSTAT C5
FDA Adverse Event
Malfunction
·RESPIRONICS NOVAMETRIX, LLC·Product code CCK·December 5, 2019