22 results
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20ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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AdvanDx Quick FISH Fixation Kit for BC ( Blood Cultures), 50 tests. In vitro diagnostic. The QuickFISH Fixation Kits are components that are sold separately for the Staphylococcus QuickFISH BC test Catalog number: QFFixBC1-50 (a component for QFSTABC1-50)
FDA Recall
Terminated
·Advandx Inc·Product code NXX·July 4, 2014
Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system
FDA Recall
Terminated
·GE Healthcare, LLC·Product code LLZ·August 12, 2021
Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·October 13, 2021
Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep.
FDA Enforcement
Class II
·Terminated·NOX MEDICAL·October 13, 2021
Diana Automated Compounding System, Diana Onco 3xx, Item No. ASN303 The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.
FDA Enforcement
Class II
·Terminated·ICU Medical, Inc.·April 20, 2016
GE Centricity PACS-IW versions 3.6.0 through 3.7.3.9 SP1, SP2, SP3 and 3.7.3 SPa10, Model Numbers: a) 2052831-00x b) 2050578-0xx c) 2090228-002 d) 2052782-00x
FDA Recall
Terminated
·GE Healthcare, LLC·Product code LLZ·May 22, 2019
GE Centricity PACS-IW versions 3.6.0 through 3.7.3.9 SP1, SP2, SP3 and 3.7.3 SPa10, Model Numbers: a) 2052831-00x b) 2050578-0xx c) 2090228-002 d) 2052782-00x
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·June 19, 2019
MYLA server HP Proliant: DL380-G8 and ML350-G6 version 3.xx computer application software. MYLA V3 is a computer application ("Middleware") based on Web 2.0 technology which: Interfaces between the instruments connected to the application and the LIS(s) (Laboratory Information System(s).
FDA Enforcement
Class II
·Terminated·bioMerieux, Inc.·May 27, 2015
Diana Automated Compounding System, Diana Onco 3xx, Item No. ASN303 The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.
FDA Recall
Terminated
·ICU Medical, Inc.·Product code NEP·March 8, 2016
MYLA server HP Proliant: DL380-G8 and ML350-G6 version 3.xx computer application software. MYLA V3 is a computer application ("Middleware") based on Web 2.0 technology which: Interfaces between the instruments connected to the application and the LIS(s) (Laboratory Information System(s).
FDA Recall
Terminated
·bioMerieux, Inc.·Product code N/A·April 14, 2015
Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep.
FDA Recall
Terminated
·NOX MEDICAL Keldnaholt Reykjavik Iceland·Product code MNR·September 7, 2021
VIPA Veronikis Intra-Fiberoptic Pelvic Assistant, Set Catalog No 350-370. VIPA Set Includes: VIPA Urethropexy Tip Catalog No. 350-374 (Also sold individually); VIPA Urethropexy Elbow Catalog No. 350-375 (also sold individually); VIPA Vaginal Cuff Tips (small) Catalog No. 350-376 (Also sold individually); VIPA Vaginal Cuff Tips (large) Catalog No. 350-378 (Also sold individually); VIPA Rectal Probe Catalog No. 350-380 (Also sold Individually); VIPA Fiber Optic Cable (Storz to ACMI Connection) Catalog No. 350-372 (Also sold individually). For use in Urethropexy Procedures and Paravaginal Repairs (accurate suture placement by illuminating the anatomy lateral to the bladder neck); in Sacrocolpopexy (steadies the vaginal vault and provides a suture platform with fiberoptic illumination); in Vaginal surgery (illuminates the rectum to visualize endometriosis lesions on the rectovaginal septum).
FDA Recall
Terminated
·Marina Medical Instruments Inc.·Product code EXX·April 9, 2009
Magellan Robotic System; Model No(s). 11132 and 11139. A steerable catheter control system used at clinical sites.
FDA Recall
Terminated
·Hansen Medical Inc·Product code DXX·March 18, 2015
Magellan Robotic Catheter Accessory Kits, Model number MACC 50 and MACC80. Cardiology: The Hansen Medical Magellan System is a robotic control system that enables positioning and visualization of a Magellan Catheter and an off-the-shelf guide wire while allowing a physician to remain seated and away from the x-ray radiation source. The Accessory Kits contain disposable components that keep the Magellan Catheters and 3rd-party guide wires performing smoothly during system operation.
FDA Recall
Terminated
·Hansen Medical Inc·Product code DXX·March 25, 2016
Artisan brand Extend Control Catheter; An Steerable Guide Catheter; Component of Sensei X Robotic Catheter System; Model Number: 07546; Distributed and Manufactured by Hansen Medical, Inc, Mountain View, CA
FDA Recall
Terminated
·Hansen Medical Inc·Product code DXX·October 19, 2009
Sensei X Robotic Catheter System, model numbers 02057 and 08257. - Set up joint (SUJ)mechanical clamp that secures the SUJ to the catheter laboratory table. Product Usage: The Sensei X Robotic Catheter System is an electromechanical software controlled system designed to facilitate navigation and control of Hansen Medicals robotically steerable catheters for collecting electrophysiological data within the heart atria with electro-anatomic mapping and recording systems.
FDA Recall
Terminated
·Hansen Medical Inc·Product code DXX·December 4, 2014
HydroDot brand: Wave Prep Single use cups, 8.5 gm (0.3 oz) 24/box-Product 1700-24 - Product Usage: An electroconductive cream for use with external electrodes to reduce the impedance of the contact between the electrode surface and the skin. The cream is not intended for use with stimulating electrodes.
FDA Recall
Terminated
·Bio-Signal Group Corp.·Product code KOY·October 29, 2019
HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03. An electroconductive cream for use with external electrodes - Product Usage: An electroconductive cream for use with external electrodes to reduce the impedance of the contact between the electrode surface and the skin. The cream is not intended for use with stimulating electrodes.
FDA Recall
Terminated
·Bio-Signal Group Corp.·Product code KOY·October 29, 2019
Medisystems 15 Gauge x 3/5 inch Buttonhole Needle Set Product Code: BH-2035PE Product Usage: Medisystems Buttonhole Needle Sets are indicated for use as an access device for dialysis and pheresis procedures using a constant site orbuttonhole method of needle insertion.
FDA Recall
Terminated
·Medisystems a NX Stage Company·Product code FIE·December 20, 2012
Medisystems 17 Gauge x 1" inch AV Fistula Needle Product Code: D9-2007MGLB Product Usage: Medisystems AVF with MasterGuard anti-stick needle protector is indicated for use as a vascular access device in hemodialysis or other extracorporeal procedures. It is intended for use in conjunction with a blood tubing set equipped with a standard medical male luer-locking connector
FDA Recall
Terminated
·Medisystems a NX Stage Company·Product code FIE·December 20, 2012