Rayner Intraocular Lenses Limited Recalls

Overview of recall records associated with Rayner Intraocular Lenses Limited, including dates, categories and classifications where available.

2recall records

Apr 29, 2020latest record date

Oct 10, 2018earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceApr 29, 2020

Rayner Intraocular Lenses RaySert PLUS RSP01 recall — FDA Z-1753-2020

RaySert PLUS RSP01 LOT K030 labeled with an expiry of 2024-01 contained an inner tray that was labeled with an expiry of 2015. In addition to having an expiry of 2015 the LOT number on the…

Class IIFDA: OngoingRayner Intraocular Lenses Limited

Medical DeviceOct 10, 2018

Rayner Intraocular Lenses C-flex 570C +19.0D Intraocular Lens Product Usage: C-flex IOLs are recall — FDA Z-3282-2018

Firm become aware of reports of post-operative refractive errors following implantation of lenses.

Class IIFDA: TerminatedRayner Intraocular Lenses Limited

Understanding this recall history

This page summarizes recall records in which the official source identifies Rayner Intraocular Lenses Limited 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.