Medical Device Control Office

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Medical device alert on a blood glucose monitoring system (Posted 18 May 2012)

Safety alert over Cameron Health SQ-RX Pulse Generators (Posted 25 April 2012)

Safety alert over certain Medtronic implantable cardioverter-defibrillators (Posted on 6 March 2012)

Recall of EUKARE Blood Glucose Test Strip (Posted on 5 March 2012)

Recall of Mylife Pura blood glucose strips in France (Posted on 22 February 2012)

Recall of Cardiac Science automated external defibrillators (Posted on 31 January 2012)

Recall of selected lots of ACUVUE® OASYS® with HYDRACLEAR® Plus Contact Lenses (Posted on 10 January 2012)

DH maintains vigilance over safety of PIP breast implants (Posted on 9 January 2012)

Recommendation by the French authority on removal of PIP breast implants (Posted on 23 December 2011)

Adverse events related to Poly Implant Prothese breast implants (Posted on 23 December 2011)

Safety alert over Lenscare SH- Monatslinsen contact lenses (7 December 2011)

Recall of Merz Aesthetics' Radiesse Dermal Filler (Posted on 25 November 2011)

Recall of FreshKon Airis 1-Month contact lenses (Posted on 18 November 2011)

Recall of Avaira and BioComfort XO contact lense (Posted on 16 November 2011)

Safety alert over Abbott's FreeStyle InsuLinx Blood Glucose Monitoring System (Posted on 2 November 2011)

Safety Alert on Two St Jude Medical's Pacemakers - Accent DR and Anthem CRT-P (Posted on 23 Sept 2011)

Alert over an HIV home test kit (Posted on 16 September 2011)

Safety alert on ShoulderFlex massager (26 August 2011)

Recall of Avaira Toric and BioComfort XO Toric contact lenses (Posted on 22 August 2011)

Suspend use of Avaira Toric daily contact lenses advisable (Posted on 20 August 2011)

Recall of Bayer's Coutour and Contour TS Glucose Test Strips (17 Aug 2011)

Recall of two Mona Lisa intrauterine contraceptive devices (with photo) (29 Jul 2011)

Recall of Alterna® Sterile Post-Operative ostomy bags due to sterility problem (28 Jul 2011)

Alert on performance of two automated external defibrillators (Posted on 23 June 2011)

Safety alert over Roche blood glucose strip (Posted on 21 June 2011)

Safety alert over certain Cameron pulse generators (7 June 2011)

Recall of Braunoderm disinfectant solution (23 May 2011)

Alert on voluntary recall and corrective action by Defibtech on semi-automatic external defibrillators (4 May 2011)

Recall of microbial contaminated protective wipes and adhesive removers (Posted on 15 April 2011)

Safety alert on ACCU-CHEK FlexLink Plus infusion sets (Posted on 2 March 2011)

Safety concern on Fraxel re:store Dual Laser System (Posted on 11 February 2011)

Serious safety concern on some Medico implantable pacemakers (Posted on 27 January 2011)

Resumption of Sale of Abbott's Optium Omega glucose test strips (Posted on 11 January 2011)

Blanket recall of Abbott glucose test strips (Posted on 29 December 2010)

Recall of Abbott’s Glucose Test Strips (Posted on 23 December 2010)

Further Recall of Single-Use Contact lenses (Posted on 28 October 2010)

Contact lens problems (Posted on 23 August 2010)

Voluntary Recall of Single-Use Contact Lenses (Posted on 20 August 2010)

Recall of automated peritoneal dialysis system (Posted on 11 August 2010)

Caution on Novabel Dermal Filler (Posted on 2 August 2010)

Software defect may cause malfunction in implantable cardioverter-defibrillator (Posted on 9 June 2010)

Recall of automated external defibrillators (Posted on 3 June 2010)

Software defect causes malfunction in implantable cardioverter-defibrillator (Posted on 7 May 2010)

Software Defects Cause Malfunctioning in Medtronic's Implantable Cardiac Devices (Posted on 6 May 2010)

Recall of silicone-filled breast implants (Posted on 1 April 2010)

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)

Recall of Automated External Defibrillators (Posted 24 April 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)

Update on cases of fungal corneal infections (Posted 16 May 2006)

Update on cases of fungal corneal infections (Posted 3 May 2006)

Update on advice for prevention of fungal corneal infections (Posted 24 April 2006)

Seek professional medical advice before breast augmentation (Posted 13 April 2006)

Update on cases of fungal corneal infections (Posted 13 April 2006)

Update on cases of fungal corneal infections (Posted 4 March 2006)

DH keeps close watch on fungal corneal infections in Singapore (Posted 22 February 2006)

Public reminded to clean contact lens properly (Posted 18 February 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)

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Last revision date: 21 March 2012