12 Sep 2024 |
DH follows up on adverse event reported by Hospital Authority |
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05 Nov 2023 |
DH follows up Field Safety Corrective Action notice by Olympus Hong Kong and China Limited |
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25 Feb 2023 |
DH follows up preliminary investigation result from local supplier of surgical lights |
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22 Jul 2021 |
Safety alert on Accu-Chek Performa test strips (with photo) |
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16 Jun 2021 |
Recall of certain models of Philips Respironics ventilators |
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26 May 2021 |
Recall of specific lots of Bausch & Lomb Ophtaxia Eye Wash (with photos) |
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28 Jul 2020 |
Cluster of Burkholderia cepacia complex infection under DH investigation (with photos) |
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10 Dec 2019 |
Safety alert on NADAL hCG Pregnancy Test |
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30 Sep 2019 |
DH monitors safety of breast implants |
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09 Sep 2019 |
DH notified of recall of specific lots of 1-Day Acuvue contact lenses |
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28 Aug 2018 |
Safety alert on specific lots of CoaguChek blood coagulation test strips (with photos) |
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23 Aug 2018 |
Further recall of Eurogine SL intrauterine devices (with photos) |
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03 May 2018 |
DH notified of recall of specific lots of Accu-Chek Performa test strips (with photos) |
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14 Mar 2018 |
Recall of Eurogine SL intrauterine devices (with photos) |
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20 Oct 2017 |
Safety alert on Biobase Medical Refrigerator |
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12 Sep 2017 |
DH notified of recall of specific lots of MiniMed Infusion Sets |
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03 Jul 2017 |
DH notified of batch recall of NovoPen Echo and NovoPen 5 |
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20 Jan 2017 |
Safety alert on automated external defibrillator LIFEPAK 1000 |
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15 Nov 2016 |
Safety alert on contamination of heater-cooler device use in cardiothoracic surgery |
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14 Jan 2016 |
Recall of two batches of One Step HCG Pregnancy Test |
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31 Dec 2015 |
Medical Device Safety Alert: Safety alert on Cardiac Science defibrillation electrodes (with photo) |
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15 Apr 2015 |
Recall of syringe slip tip (with photo) |
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20 Jan 2015 |
Safety alert on component of peritoneal dialysis system (with photos) |
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15 Jul 2014 |
Safety alert on Cellnovo insulin infusion set |
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12 Jun 2014 |
Safety alert over Advocate Redi-Code+ blood glucose test strip |
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30 Apr 2014 |
Safety alert over GenStrip Blood Glucose Test Strips |
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10 Apr 2014 |
Safety alert over certain brands of Roche Diabetes Care blood glucose test strips and blood glucose monitoring systems |
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03 Mar 2014 |
Recall of certain brands of Abbott Diabetes Care blood glucose monitoring systems |
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20 Jan 2014 |
Safety alert on insulin cartridges of t:slim Insulin Pump |
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04 Dec 2013 |
Safety alert on Philips HeartStart FRx and HeartStart HS1 automated external defibrillators |
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28 Nov 2013 |
Further recall of FreeStyle and FreeStyle Lite blood glucose test strips |
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26 Nov 2013 |
Further recall of selected lots of FreeStyle Lite blood glucose test strips |
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25 Nov 2013 |
Recall of certain lots of FreeStyle and FreeStyle Lite blood glucose test strips |
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20 Nov 2013 |
Safety alert on three Sorin pacemakers |
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19 Nov 2013 |
Safety alert over Lenscare SH-System Monatslinsen monthly contact lenses |
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30 Jul 2013 |
Recall of Nova Max Glucose Test Strips |
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06 Jul 2013 |
Safety alert on GE Healthcare nuclear medicine systems |
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06 May 2013 |
Safety alert on CoaguChek blood coagulation testing devices |
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24 Apr 2013 |
Recall of PTS Panels Glucose Test Strips (with photo) |
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10 Apr 2013 |
Safety alert on automated peritoneal dialysis system |
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27 Mar 2013 |
Recall of Multiload Radiopaque Cu375 intrauterine contraceptive devices (with photos) |
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22 Mar 2013 |
Safety alert on two automated external defibrillators |
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21 Feb 2013 |
Recall of Restylane SubQ Lidocaine 2ml dermal filler |
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15 Jan 2013 |
Recall of selected lots of two brands of Acuvue contact lenses |
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17 Jul 2012 |
Safety alert on ear lubricant |
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18 May 2012 |
Medical device alert on a blood glucose monitoring system |
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24 Apr 2012 |
Safety alert over Cameron Health SQ-RX Pulse Generators |
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06 Mar 2012 |
Safety alert over certain Medtronic implantable cardioverter-defibrillators |
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05 Mar 2012 |
Recall of EUKARE Blood Glucose Test Strip |
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22 Feb 2012 |
Recall of Mylife Pura blood glucose strips in France |
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31 Jan 2012 |
Recall of Cardiac Science automated external defibrillators |
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10 Jan 2012 |
Recall of selected lots of ACUVUE® OASYS® with HYDRACLEAR® Plus Contact Lenses |
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09 Jan 2012 |
DH maintains vigilance over safety of PIP breast implants |
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23 Dec 2011 |
Recommendation by the French authority on removal of PIP breast implants |
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22 Dec 2011 |
Adverse events related to Poly Implant Prothese breast implants |
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07 Dec 2011 |
Safety alert over Lenscare SH- Monatslinsen contact lenses |
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25 Nov 2011 |
Recall of Merz Aesthetics' Radiesse Dermal Filler |
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18 Nov 2011 |
Recall of FreshKon Airis 1-Month contact lenses |
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16 Nov 2011 |
Recall of Avaira and BioComfort XO contact lenses |
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02 Nov 2011 |
Safety alert over Abbott's FreeStyle InsuLinx Blood Glucose Monitoring System |
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23 Sep 2011 |
Safety Alert on Two St Jude Medical's Pacemakers - Accent DR and Anthem CRT-P |
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15 Sep 2011 |
Alert over an HIV home test kit |
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26 Aug 2011 |
Safety alert on ShoulderFlex massager |
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22 Aug 2011 |
Recall of Avaira Toric and BioComfort XO Toric contact lenses |
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20 Aug 2011 |
Suspend use of Avaira Toric daily contact lenses advisable |
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16 Aug 2011 |
Recall of Bayer's Contour and Contour TS Glucose Test Strips |
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29 Jul 2011 |
Recall of two Mona Lisa intrauterine contraceptive devices (with photo) |
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28 Jul 2011 |
Recall of Alterna® Sterile Post-Operative ostomy bags due to sterility problem |
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23 Jun 2011 |
Alert on performance of two automated external defibrillators |
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21 Jun 2011 |
Safety alert over Roche blood glucose strip |
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07 Jun 2011 |
Safety alert over certain Cameron pulse generators |
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23 May 2011 |
Recall of Braunoderm disinfectant solution |
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04 May 2011 |
Alert on voluntary recall and corrective action by Defibtech on semi-automatic external defibrillators |
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15 Apr 2011 |
Recall of microbial contaminated protective wipes and adhesive removers |
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02 Mar 2011 |
Safety alert on ACCU-CHEK FlexLink Plus infusion sets |
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11 Feb 2011 |
Safety concern on Fraxel re:store Dual Laser System |
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27 Jan 2011 |
Serious safety concern on some Medico implantable pacemakers |
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11 Jan 2011 |
Resumption of Sale of Abbott's Optium Omega glucose test strips |
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29 Dec 2010 |
Blanket recall of Abbott glucose test strips |
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23 Dec 2010 |
Recall of Abbott's glucose test strips |
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27 Oct 2010 |
Further Recall of Single-Use Contact Lenses |
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20 Aug 2010 |
Contact lens problems |
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19 Aug 2010 |
Voluntary Recall of Single-Use Contact Lenses |
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11 Aug 2010 |
Recall of automated peritoneal dialysis system |
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31 Jul 2010 |
Caution on Novabel Dermal Filler |
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09 Jun 2010 |
Software defect may cause malfunction in implantable cardioverter-defibrillator |
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01 Jun 2010 |
Recall of automated external defibrillators |
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06 May 2010 |
Software defect causes malfunction in implantable cardioverter-defibrillator |
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05 May 2010 |
Software Defects Cause Malfunctioning in Medtronic's Implantable Cardiac Devices |
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31 Mar 2010 |
Recall of silicone-filled breast implants |
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12 Feb 2010 |
Recall of LifeScan OneTouch SureStep blood glucose test strips with incorrect readings |
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18 Nov 2009 |
Field Correction of Automated External Defibrillators |
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08 Sep 2009 |
Heartbeat regulating products with low-voltage problem |
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19 May 2009 |
Follow-up Action on Medtronic Kappa and Sigma Pacemakers |
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24 Apr 2009 |
Recall of Automated External Defibrillators |
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23 Apr 2009 |
Recall of blood glucose meters with incorrect readings (i-sens Model CareSens II) |
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23 Apr 2009 |
Voluntary recall of device containing non-sterile radioactive material |
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15 Oct 2007 |
Voluntary Suspension of Defibrillation Leads |
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11 Sep 2007 |
Medical Device Alert for Blood Glucose Meters |
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26 May 2007 |
Recall of AMO Contact Lens Solution |
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25 Apr 2007 |
Recall of Medical Device for Treatment of Temporary Stoppage of Breathing during Sleep (CPAP Machines) |
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13 Apr 2007 |
Advisory Notice on Use of Heartbeat Regulating Products |
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19 Dec 2006 |
DH closely monitoring safety of Lifescan blood glucose meter |
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23 Nov 2006 |
DH and Customs keep close watch on recall of contact lens solutions |
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22 Nov 2006 |
DH monitoring recall of four AMO contact lens solution |
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19 Oct 2006 |
Software problem found in programming devices for implantable pacemakers |
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27 Jun 2006 |
Voluntary Recall of Heartbeat Regulating Products |
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16 May 2006 |
Update on cases of fungal corneal infections |
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03 May 2006 |
Update on cases of fungal corneal infections |
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24 Apr 2006 |
Update on advice for prevention of fungal corneal infections |
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13 Apr 2006 |
Seek professional medical advice before breast augmentation |
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13 Apr 2006 |
Update on cases of fungal corneal infections |
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04 Mar 2006 |
Update on cases of fungal corneal infections |
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22 Feb 2006 |
DH keeps close watch on fungal corneal infections in Singapore |
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18 Feb 2006 |
Public reminded to clean contact lens properly |
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18 Jan 2006 |
DH notified of intra-uterine contraceptive device cases |
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24 Dec 2005 |
Update on Removal of Contraceptive Device |
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13 Dec 2005 |
Removal of Contraceptive Device |
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01 Dec 2005 |
Follow-up Action on Medtronic Sigma® Pacemakers |
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14 Nov 2005 |
Voluntary Listing System extended to cover medium-risk medical devices |
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03 Nov 2005 |
Voluntary Recall of Two Models of Omron® 3-Way Instant Thermometers by Omron Healthcare, Inc. |
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10 Oct 2005 |
Safety Information regarding St. Jude Medical Implantable Cardioverter Defibrillators |
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23 Sep 2005 |
Safety Information regarding Guidant INSIGNIA and NEXUS Implantable Cardiac Pacemakers |
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19 Jul 2005 |
Corrective Action of Guidant implantable cardiac pacemakers |
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18 Jun 2005 |
Voluntary Recall of Implantable Cardiac Defibrillators by Guidant Corporation |
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26 Nov 2004 |
Administrative control of medical devices to be launched in phases |
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