Rayner Intraocular Lenses RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems recall — FDA Z-1338-2022
The outer package is mislabeled and the package contains a different IOL strength.
Overview of recall records associated with Rayner Intraocular Lenses Ltd, including dates, categories and classifications where available.
Classification mix: Class II: 1.
The outer package is mislabeled and the package contains a different IOL strength.
This page summarizes recall records in which the official source identifies Rayner Intraocular Lenses Ltd as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.