Cytocell recalls 8 Square Template Slides with incorrect expiry date labels. The correct expiry is February 2022, not May 2023 as shown. Affected items may expire prematurely.
Labelled with an incorrect expiry date on the outer label with an extended expiry date than the validated shelf life. The correct expiry date for the device is 2022-02 and not 2023-05 as shown on the outer label.
Cytocell is recalling glass microscope slides that have an incorrect expiry date label showing May 2023 instead of the correct February 2022. This could cause the slides to expire before they should, potentially leading to ineffective use in scientific work.
The slides have an outer label showing an expiry date of May 2023, but the correct expiry is February 2022. This incorrect label means the slides could expire prematurely, making them ineffective for scientific use before their intended shelf life ends.
Users of Cytocell 8 Square Template Slides (glass microscope slides) with the reference PCN008 and lot number 210511-018 are affected. Researchers and students using these slides for lab work are most at risk of using expired materials.
Check for the product name 'Cytocell 8 Square Template Slides (Glass)' with reference PCN008 and lot number 210511-018. The outer label shows an expiry date of May 2023 instead of February 2022.
Verify the outer label shows an expiry date of May 2023 instead of February 2022.
The recall is happening because the outer label shows an incorrect expiry date of May 2023 instead of the correct February 2022.
The official recall record does not specify any remedy steps for affected items.
Check for the product name 'Cytocell 8 Square Template Slides (Glass)' with reference PCN008 and lot number 210511-018. The outer label shows an expiry date of May 2023 instead of February 2022.
We’ve drafted a message you can send Cytocell to request your refund or repair — edit it as you like.
Subject: Recall Z-0824-2022 — Cytocell Cytocell Hello, I own a Cytocell that is covered by recall Z-0824-2022 from Cytocell. 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.
