Press Release
Recall of LifeScan OneTouch SureStep blood glucose test strips with incorrect readings (Posted on 17 February 2010)
Field Correction of Automated External Defibrillators (Posted on 19 November 2009)
Heartbeat Regulating Products with Low-voltage Problem (Posted on 9 September 2009)
Follow-up Action on Medtronic Kappa and Sigma Pacemakers (Posted on 19 May 2009)
Voluntary Recall of blood glucose meters with incorrect readings (i-sens Model CareSens II) (Posted on 24 April 2009)
Voluntary recall of device containing non-sterile radioactive material (Posted on 2 May 2008)
Voluntary Suspension of Defibrillation Leads (Posted on 15 October 2007)
Medical Device Alert for Blood Glucose Meters (Posted on 11 September 2007)
Recall of AMO Contact Lens Solution (Posted on 26 May 2007)
Recall of Medical Device for Treatment of Temporary Stoppage of Breathing during Sleep (CPAP Machines) (Posted on 25 April 2007)
Advisory Notice on Use of Heartbeat Regulating Products (Posted on 13 April 2007)
DH Closely Monitoring Safety of Lifescan Blood Glucose Meter (19 December 2006)
DH and Customs Keep Close Watch on Recall of Contact Lens Solutions (23 November 2006)
DH Monitoring Recall of Four AMO Contact Lens Solutions (22 November 2006)
Software Problem Found in Programming Devices for Implantable Pacemakers (19 October 2006)
Voluntary Recall of Heartbeat Regulating Products (27 June 2006)
DH notified of intra-uterine contraceptive device cases (18 January 2006)
Update on Removal of Contraceptive Device (24 December 2005)
Removal of Contraceptive Device (13 December 2005)
Follow-up Action on Medtronic Sigma® Pacemakers (1 December 2005)
Voluntary Listing System extended to cover medium-risk medical devices (14 November 2005)
Voluntary Recall of Two Models of Omron® 3-Way Instant Thermometers by Omron Healthcare, Inc. (3 November 2005)
Safety Information regarding St. Jude Medical Implantable Cardioverter Defibrillators (10 October 2005)
Safety Information: Guidant INSIGNIA and NEXUS Implantable Cardiac Pacemakers (23 September 2005)
Corrective Action of Guidant implantable cardiac pacemakers (19 July 2005)
Medical Device Administrative Control System (launched on 26 November 2004)
Voluntary Recall of Implantable Cardiac Defibrillators by Guidant Corporation (18 June 2005)
2005
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Important notices
Last revision date: 17 February 2010
| Important notices
