Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Recalled by Rayner Intraocular Lenses Limited Due to RaySert PLUS RSP01 LOT K030 labeled with an...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Rayner Intraocular Lenses Limited directly.
Affected Products
RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Usage: The single use injectors (Model STWOl and Model RSPOl) are intended to be used to compress and insert into the capsular bag only those intraocular lenses that allow the use of these injectors in their approved labelling.
Quantity: 2425 Units.
Why Was This Recalled?
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 inner tray is identified as V001.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Rayner Intraocular Lenses Limited
Rayner Intraocular Lenses Limited has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report