58 results · 11ms · Sources: EU EUDAMED, US FDA

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Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are considered to be candidates for implantation of a penile prosthesis.

FDA Recall
Terminated ·Coloplast Manufacturing US, LLC·Product code FHW·October 23, 2020

Coloplast Titan OTR Inflatable Penile Prosthesis,18cm scrotal Bioflex cylinder set w/OTR Pump, P/N QSR9181400. Sterile EO. Manufacturer: Coloplast A/S, 3050 Denmark. Distributed by: Coloplast Corp., Minneapolis, MN 55411 USA. Indicated for male patients suffering from erectile dysfunction who are considered to be candidates for implantation of a penile prosthesis.

FDA Recall
Terminated ·Coloplast Manufacturing US, LLC·Product code FHW·October 6, 2009

Torosa Saline-Filled Testicular Prosthesis (Size Small)

FDA Recall
Terminated ·Coloplast Manufacturing US, LLC·Product code FHW·November 9, 2021

CytoScan¿ Dx Assay. The CytoScan Dx Assay consists of five reagent modules, wash buffers (WS), a microarray kit, and analysis software. The CytoScan Dx Assay consists of five reagent modules, wash buffers (WS), a microarray kit, and analysis software: MOD R LA, CytoScan¿ Dx Pre-PCR (-20¿C) MOD T E W, CytoScan¿ Dx Pre-PCR (2¿-8¿C) MOD F L H, CytoScan¿ Dx Post-PCR (-20¿C) MOD S AH W PB, CytoScan¿ Dx Post-PCR (2¿-8¿C) MOD E PW, CytoScan¿ Dx Post-PCR (15¿- 30¿ C) CytoScan Dx WS A CytoScan Dx WS B CytoScan¿ Dx Array kit, 6Pk ChAS Dx Analysis Software and Browser

FDA Enforcement
Class III ·Terminated·Affymetrix Inc·June 8, 2016

CytoScan Dx Assay. The CytoScan Dx Assay consists of five reagent modules, wash buffers (WS), a microarray kit, and analysis software. The CytoScan Dx Assay consists of five reagent modules, wash buffers (WS), a microarray kit, and analysis software: MOD R LA, CytoScan Dx Pre-PCR (-20C) MOD T E W, CytoScan Dx Pre-PCR (2-8C) MOD F L H, CytoScan Dx Post-PCR (-20C) MOD S AH W PB, CytoScan Dx Post-PCR (2-8C) MOD E PW, CytoScan Dx Post-PCR (15- 30 C) CytoScan Dx WS A CytoScan Dx WS B CytoScan Dx Array kit, 6Pk ChAS Dx Analysis Software and Browser

FDA Recall
Terminated ·Affymetrix Inc·Product code PFX·April 14, 2016

microTargeting" STar" Drive System (Motorized), Product Number 70-ZD-ME

FDA Recall
Terminated ·FHC, Inc.·Product code HAW·May 10, 2018

microTargeting" Lead Adapter for STar" Drive, Product Number 70-CN-DB

FDA Recall
Terminated ·FHC, Inc.·Product code HAW·May 10, 2018

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

FHC 66-ZD-MD microTargeting Drive System: System for Stereotactic Positioning Used with the Power Assist (66-DA-ME) or Display Assembly (66-DA-EN)

FDA Recall
Terminated ·FHC, Inc.·Product code HAW·March 14, 2005

microTargeting Drive System with Mounted Accessories Catalog numbers : 66-ZD-MD-01, MT-DS-01, FC1006 (Medtronic) Product is the FHC DBS Depth Stop Adapter, a component of the microTargeting Drive and the STar Drive. The Drives are intended to be used with commercially available stereotactic systems for neurosurgical procedures which require the accurate positioning of microelectrodes, stimulating electrodes, or other instruments in the brain or nervous system.

FDA Recall
Terminated ·FHC, Inc.·Product code HAW·March 30, 2010

microTargeting" STar" Drive System (Manual), Product Number 70-ZD-MA

FDA Recall
Terminated ·FHC, Inc.·Product code HAW·May 10, 2018

microTargeting" Drive System, Product Number MT-DS-01

FDA Recall
Terminated ·FHC, Inc.·Product code HAW·May 10, 2018

FHC Guideline 4000 5.0 GL5 Main Processing Unit - Product Usage: intended to record and stimulate electrophysiological activity, as well as aid in the accurate placement of electrodes and other instruments. Catalogue Number: C0215 UDI: 00873263006740

FDA Recall
Terminated ·FHC, Inc.·Product code GZL·June 17, 2020

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

Depth Stop Adapter 66-AC-DS(1.8), E6-01-.5 used with the microTargeting and STar Drives Product is the FHC DBS Depth Stop Adapter, a component of the microTargeting Drive and the STar Drive. The Drives are intended to be used with commercially available stereotactic systems for neurosurgical procedures which require the accurate positioning of microelectrodes, stimulating electrodes, or other instruments in the brain or nervous system.

FDA Recall
Terminated ·FHC, Inc.·Product code HAW·March 30, 2010

microtargeting" Depth Stop Adapter, Product Model Number, Product Number 66-AC-DS(1.8),

FDA Recall
Terminated ·FHC, Inc.·Product code HAW·May 10, 2018

FC4000 MicroTargeting Electrode Kit 5x For use with Nexframe and Nexdrive Distributed by Medtronic Inc., Minneapolis, MN REF: FCH 4000 (5 Prefilled single use kits -5 packages and 2 electrodes each) Intended for use in intra-operative recording of single unit neuronal activity or intra-operative stimulation of neural elements in the brain.

FDA Recall
Terminated ·FHC, Inc.·Product code GZL·October 20, 2008

microTargeting Drive DBS Lead Holder 66-CN-DB Product is the FHC DBS Depth Stop Adapter, a component of the microTargeting Drive and the STar Drive. The Drives are intended to be used with commercially available stereotactic systems for neurosurgical procedures which require the accurate positioning of microelectrodes, stimulating electrodes, or other instruments in the brain or nervous system.

FDA Recall
Terminated ·FHC, Inc.·Product code HAW·March 30, 2010

FHC microTargeting Platform DBS Measuring Fixture, a component of the micro-targeting Drive System (Catalog Number 66-FA-SF). The device is a stereotactic instrument used for the placement of recording and stimulating electrodes in the brain.

FDA Recall
Terminated ·FHC, Inc.·Product code HAW·October 8, 2008

FHC MicroTargeting Electrode, MTDWBP(AR)(MP I ) Intended for use in intra-operative recording of single unit neuronal activity or intra-operative stimulation of neural elements in the brain.

FDA Recall
Terminated ·FHC, Inc.·Product code GZL·October 20, 2008