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Lower risk Medical device recall · FDA · Published February 14, 2022

Cytocell 8 Square Template Slides Recall: Incorrect Expiry Date Label

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.

🇺🇸 FDA recall #Z-0824-2022Medical deviceCytocell ›
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Recalling firmCytocell Ltd.418 Cambridge Science Park, Milton Road, Oxford Gene Technology · Cambridge, United Kingdom
✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/61143-cytocell-8-square-template-slides-recall-incorrect-expiry-date-label.

Source Summary by GovInfoNow · govinfonow.com/recall/61143-cytocell-8-square-template-slides-recall-incorrect-expiry-date-label · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0824-2022

Cite this page

“Cytocell 8 Square Template Slides Recall: Incorrect Expiry Date Label.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61143-cytocell-8-square-template-slides-recall-incorrect-expiry-date-label. Based on FDA recall #Z-0824-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0824-2022%22&limit=1).

The FDA announced on Feb. 14, 2022, that Cytocell Ltd. voluntarily recalled Cytocell 8 Square Template Slides (Glass) microscope slides due to an incorrect expiry date on the outer label. The company initiated the recall after discovering the label showed an extended date of May 2023 instead of the validated Feb. 2022.

How to tell if you have it

  • Brand: Cytocell
  • Product: Cytocell 8 Square Template Slides (Glass)- microscope slides
  • Reference: PCN008
  • Lot code: 210511-018
  • Quantity: 5 kits
  • Distribution: US Nationwide in CT and TX

The hazard

The device was labelled with an incorrect expiry date on the outer label, showing an extended expiry date of May 2023 rather than the validated shelf life ending in Feb. 2022.

Context

GovInfoNow's records show Cytocell Ltd. has had 12 other recalls since March 15, 2019. Recent brand recalls include a May 24, 2023 recall for RET Distal Probe due to DNA inversion risk and two Oct. 27, 2022 recalls involving BCL11B reagent mislabeling and probe mapping errors. Other recent recalls of similar products include Cardinal Health ChemoPlus Gowns Recall (Nov. 12, 2025), Inspire Stimulation Lead Recall (May 11, 2026), and B Braun Discofix Four Way Stopcock Recall (Aug. 4, 2026).

How to tell if you have this one

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.

  • Brand
    Cytocell
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Expiry Date

    Verify the outer label shows an expiry date of May 2023 instead of February 2022.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 2 states.

Alaska: nationwideAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: nationwideWAIdaho: nationwideIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: nationwideILWisconsin: nationwideWIMichigan: nationwideMINew York: nationwideNYRhode Island: nationwideRIMassachusetts: nationwideMAOregon: nationwideORNevada: nationwideNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: nationwideIAIndiana: nationwideINOhio: nationwideOHPennsylvania: nationwidePANew Jersey: nationwideNJConnecticut: named in the noticeCTCalifornia: nationwideCAUtah: nationwideUTColorado: nationwideCONebraska: nationwideNEMissouri: nationwideMOKentucky: nationwideKYWest Virginia: nationwideWVVirginia: nationwideVAMaryland: nationwideMDDelaware: nationwideDEArizona: nationwideAZNew Mexico: nationwideNMKansas: nationwideKSArkansas: nationwideARTennessee: nationwideTNNorth Carolina: nationwideNCSouth Carolina: nationwideSCDistrict of Columbia: nationwideDCOklahoma: nationwideOKLouisiana: nationwideLAMississippi: nationwideMSAlabama: nationwideALGeorgia: nationwideGAHawaii: nationwideHITexas: named in the noticeTXFlorida: nationwideFL

FDA distribution: “US Nationwide distribution in the states of CT, TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Connecticut, Texas.

Recall timeline

FDA terminated this recall 16 months after the firm started it.

1. Firm started the recall: Feb 14, 202212. FDA classified it Class III: Mar 24, 202223. Published in FDA’s Enforcement Report: Mar 30, 202234. FDA terminated the recall: Jun 12, 2023420222023
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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.

  • Official source: FDA Recall #Z-0824-2022 (February 14, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0824-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA