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Originator: MHRA Medical Device Alerts

Issue date: 13-Feb-2019 12:02:01

This alert has been issued to:
  • Care Trusts
  • Mental Health Trusts
  • Specialists Trusts
  • NHS Regional Offices
  • Learning Disabilities Trusts
  • Mental Health & Social Care Trusts
  • Ambulance Trusts
  • Mental Health & Learning Disabilities Trusts
  • Acute Trusts
  • Community Trusts

  • Other contacts
  • Independent Healthcare Providers (registered with CAS)
  • Clinical Commissioning Groups
  • Social Care Providers (registered with CAS)
  • Special Health Authorities

Action category: Action

Title: Ophthalmic implant Raindrop Near Vision Inlay – risk of corneal haze.

Broadcast content: Manufactured by ReVision Optics, Inc – patients implanted with this device have an increased risk of corneal haze.

Additional information: NHS England Regional Offices: please cascade to GP Practices and Optometrists.

Alert reference: MDA/2019/007

Action underway deadline: 27-Feb-2019

Action complete deadline: 10-Apr-2019

Attachments:

Contact our helpdesk

Email: safetyalerts@mhra.gov.uk

Medicines and Healthcare products Regulatory Agency