29 results
·
53ms
·
Sources: EU EUDAMED, US FDA
DYNATORQUE ATTACHMENT
FDA Adverse Event
Other
·PRO-DEX MICRO MOTORS INC.·Product code EFB·October 15, 2013
MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code HBC·January 20, 2017
MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code HBC·January 20, 2017
SANAO
FDA Adverse Event
Injury
·SCICAN GMBH·Product code EGS·March 20, 2015
1/2 SIZE PERF BASKET LID 247X257MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code FSM·June 8, 2017
1/2 SIZE PERF BASKET LID 247X257MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code FSM·June 8, 2017
1/2 SIZE PERF BASKET LID 247X257MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code FSM·June 8, 2017
MICROSPEED UNI MICRO 150 MOTOR
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code HBC·April 7, 2016
MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 10, 2022
MICROSPEED UNI CONTROL UNIT W/COOL.UNIT
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code HBC·July 3, 2008
MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code HWE·June 8, 2017
MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code HWE·June 8, 2017
MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code HWE·June 8, 2017
MICRO-LINE STRAIGHT HDPC 1:1 ROUND SHAFT
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code HWE·June 21, 2017
Medtronic microTargeting Drive Motor Option used with the micro Targeting Drive System with models: 9033G0711; 9033G0712; 9033G0713; 9033G0811 and FHC 1008-66
FDA Recall
Terminated
·FHC, Inc.·Product code HAW·October 31, 2005
MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code HWE·March 2, 2016
FHC microTargeting Power Assist System used with the micro Targeting Drive System, models: 66-DA-ME; 66EL-MC; 66EL-MS;66EL-MS-02; 66-EL-MS-03; 66-EL-RM; MT-DS-AM; MT-DS-MD.
FDA Recall
Terminated
·FHC, Inc.·Product code HAW·October 31, 2005
A1A-2000
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·March 29, 2018
PUMP MMT-1781K 670G V4.11 MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·September 3, 2021
DAVINCI X
FDA Adverse Event
Injury
·INTUITIVE SURGICAL, INC·Product code NAY·October 18, 2023