Last updated: October 2, 2026
The Raindrop Near Vision Inlay is an obsolete corneal implant and is not presented by Fichte, Endl & Elmer Eyecare as a currently available vision correction option. Historical promotional articles on this website have been retired and redirected to this notice.
FDA Recall Information
The U.S. Food and Drug Administration classified a recall of all unused Raindrop Near Vision Inlay units as Class I after a post-approval study identified an increased risk of corneal haze following implantation. The recall was initiated in November 2018, posted by the FDA in March 2019, and later listed as terminated in March 2024. A terminated recall status does not mean the device has returned as a current treatment option.
Read the FDA Class I recall record.
For Patients Who Previously Received the Inlay
Patients who previously received a Raindrop Near Vision Inlay should continue care with an ophthalmologist familiar with their eye history. Do not make treatment decisions based only on older promotional content. Bring implant records, operative reports, prior measurements, and the names of any treating clinicians to the visit when available.
Contact an eye-care professional promptly for new or worsening haze, glare, halos, visual fluctuation, pain, redness, light sensitivity, or loss of vision. Severe pain, sudden vision loss, injury, or a very red eye may require urgent or emergency evaluation.
Current Vision Correction Evaluation
Patients seeking help with reading vision or age-related near-vision changes can review current laser and lens-based vision correction options. The appropriate approach depends on age, prescription, corneal measurements, lens changes, eye health, medical history, visual priorities, and the risks and limitations of each available treatment.
Call 1-800-309-2020 or request an appointment for an individualized evaluation.
This notice provides general education and does not replace an examination or advice from a treating ophthalmologist.
