International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

Name	Date initiated	Country	Source
Recall of Lipase Reagent (diagnostic good for the quantitation of lipase in human serum or plasma)	2014-04-09	Australia	DHTGA
Recall of LenSx Laser System (used for femtosecond cataract surgery)	2014-04-10	Australia	DHTGA
Recall of syngo Dynamics v9.5 with Sensis-syngo Dynamics Integration (Radiology picture archiving and communication system)	2014-04-17	Australia	DHTGA
Recall of MEDRAD Continuum Infusion PumpSystems ditributed prior to March 2008	2014-04-11	Australia	DHTGA
Recall of EverCross .035" OTW PTA Catheter (Balloon dilatation angioplasty catheter)	2014-04-10	Australia	DHTGA
Recall of Extension Tubing in Refill Kits for use with Synchromed pumps	2014-04-11	Australia	DHTGA
Recall of DigitalDiagnost (Digital X-ray System)	2014-04-11	Australia	DHTGA
Recall of Infant Nasal CPAP Prongs and Bubble CPAP Starter Kits	2014-04-14	Australia	DHTGA
Recall of Accu-Chek Mobile Blood Glucose Monitoring System	2014-04-17	Australia	DHTGA
Recall of ExacTrac 5.5.5 (Image guided radiation therapy patient positioning system)	2014-04-14	Australia	DHTGA
Recall of ADVIA Centaur, ADVIA Centaur XP and ADVIA Centaur CPADVIA Centaur Systems TSH3 Ultra 100T, 500T	2014-04-17	Australia	DHTGA
Recall of Centricity PACS RA1000 Workstation versions 3.2 and higher (Picture archiving and communication system)	2014-04-15	Australia	DHTGA
Recall of SynFix-LR Surgical Implant Holder	2014-04-28	Australia	DHTGA
Recall of FOLFusor SV 0.5 ml/hr	2014-04-17	Australia	DHTGA
Recall of Colied-Tube INFUSOR System	2014-04-17	Australia	DHTGA
Recall of Tension Band Pins (Internal fixation pins)	2014-05-09	Australia	DHTGA
Recall of Panda iRes Warmers integrated with Nellcor SpO2	2014-04-16	Australia	DHTGA
Recall of Cochlear Baha Soft Tissue Gauge (included in the Cochlear Baha Attract surgical tool kit)	2014-04-16	Australia	DHTGA
Recall of AQURE Data Management System Software prior to version 1.8.2 may be affected.	2014-04-17	Australia	DHTGA
Recall of Mueller Hinton-HTM (culture media). An in vitro diagnostic medical device (IVD)	2014-04-17	Australia	DHTGA
Recall of 550 TxT Treatment Table used with PRIMUS, ONCOR and ARTISTE Digital Linear Accelerators (LINAC)	2014-04-17	Australia	DHTGA
Recall of Percutaneous Sheath Introducer Kits	2014-04-28	Australia	DHTGA
Recall of Luminos dRF (Fluoroscopic diagnostic x-ray systems)	2014-04-17	Australia	DHTGA
Recall of SOMATOM Emotion 6 / 16 Slice Configuration and SOMATOM Spirit/Spirit Power Systems (Full-body computed tomography (CT) diagnostic x-ray system)	2014-04-17	Australia	DHTGA
Recall of Otto Bock A200 Power Wheelchair, SKIPPI and SKIPPI PLUS Power Wheelchairs Units delivered between 20 June 2011 and 8 March 2013	2014-04-23	Australia	DHTGA

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.