Increased risk of corneal haze in patients implanted with Raindrop Near Vision Inlays
Healthcare professional
Medical devices
4 March 2019
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Swissmed Pte Ltd would like to inform healthcare professionals of an increased risk of corneal haze caused by the ophthalmic implant Raindrop Near Vision Inlays. The post-approval study mandated by US Food and Drug Administration showed that 75% of 150 enrolled patients with implantation developed corneal haze. In 42% of patients, the corneal haze has been present in the central region of the cornea. Healthcare professionals are advised to stop the use of the affected inlays and to monitor patients who have the inlays implanted or have previously had the devices explanted for the development of corneal haze. Please refer to the letter for details.
Only abstracts of the Dear Healthcare Professional Letters (DHCPL) are provided on this website. Details of these letters can be found in the MOH Alert System, which is accessible via the Health Professionals Portal (HPP), a one-stop portal for all healthcare professionals in Singapore. Dentists, medical doctors and pharmacists may access HPP at https://hpp.moh.gov.sg and follow the procedures below to access the MOH Alert system.
Step 1: Select your profession under ‘For Healthcare Professionals’.
Step 2: Click on ‘Useful links’.
Step 3: Click on ‘MOH Alert’ and log in via Singpass.
Step 4: Click on ‘Drug Alerts’ or ‘Med Device Alerts’ to view the DHCPLs.
