Klinika Medical recalls KliniTray tissue resection margin examination boards (model 2001105-F) due to potential microbial contamination. Affected units may pose health risks if used without proper cleaning.
Potential for microbial contamination.
Klinika Medical is recalling KliniTray tissue resection margin examination boards (model 2001105-F) because they could become contaminated with microbes. This poses a health risk if the device is used without proper cleaning.
The device could become contaminated with microbes if not cleaned properly. This contamination might lead to infections if the device is used without adequate sanitation.
Medical professionals using KliniTray for surgical procedures are most at risk. The recall applies to devices with model number 2001105-F sold between specific dates.
Check for the model number 2001105-F on the device. The recall covers units sold with lot number 25.019.01.
Look for the model number 2001105-F on the device to confirm if it is affected.
The device may pose a risk of microbial contamination if not cleaned properly, so it should not be used without following the recall instructions.
Check the model number on the device. If it matches 2001105-F, contact Klinika Medical for further instructions.
Look for the model number 2001105-F and lot number 25.019.01 on the device to confirm it is affected.
We’ve drafted a message you can send Klinika Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1768-2025 — Klinika Medical Klinika Medical Hello, I own a Klinika Medical that is covered by recall Z-1768-2025 from Klinika Medical. 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.
