Rayner recalls RaySert PLUS RSP01 lenses with LOT K030 (expiry 2024-01) due to inner tray expiry date mismatch (2015). Affected users should check product labels for model STWOl or RSPOl.
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.
Rayner is recalling single-use injectors (Model STWOl and RSPOl) that have an inner tray expiring in 2015 but the outer packaging lists an expiry of 2024. This mismatch means the inner tray may have expired before use, potentially causing issues with lens insertion.
The inner tray of the product expires in 2015, but the outer packaging shows an expiry date of 2024. This mismatch could mean the inner tray has expired before the product is used, potentially affecting the lens insertion process.
Users of Rayner RaySert PLUS RSP01 single-use injectors with LOT K030 (expiry 2024-01) are affected. Those who have the specific model numbers STWOl or RSPOl are most at risk.
Check for the product model STWOl or RSPOl on the packaging. Look for the lot number K030 and the outer expiry date of 2024-01.
Verify the model number (STWOl or RSPOl) and lot number (K030) on the packaging.
The inner tray expires in 2015 while the outer packaging shows an expiry of 2024-01. This mismatch could mean the inner tray has expired before use.
Check the product labels for model STWOl or RSPOl and lot number K030. If you have these, contact Rayner for guidance.
The recall record does not specify a remedy, so no action is required beyond checking the labels.
We’ve drafted a message you can send Rayner to request your refund or repair — edit it as you like.
Subject: Recall Z-1753-2020 — Rayner Rayner Hello, I own a Rayner that is covered by recall Z-1753-2020 from Rayner. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
