CooperSurgical recalls K-Systems T47 Warming Plates with model K23054 that may overheat, causing temperature exceedance. Affected units have specific serial numbers. Contact for remedy.
The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will alarm appropriately.
CooperSurgical recalls K-Systems T47 Warming Plates with model number K23054 due to potential overheating. This could cause temperatures to exceed the set value, triggering alarms but not necessarily causing harm. The recall affects specific units with listed serial numbers.
The warming plate may overheat, causing temperatures to exceed the desired set value. The device will alarm when this happens, but the overheating itself does not cause injury or damage to users or materials.
Individuals using K-Systems T47 Warming Plates with model K23054 for assisted reproductive procedures are affected. Those handling reproductive biological materials in labs or clinics using these units are most at risk.
Check for the model number K23054 on the device. Affected units have specific serial numbers listed in the recall notice, including ranges like 2218KH46 to 2337KH10.
Look for the model number K23054 on the warming plate to confirm if it is affected.
The warming plate may overheat, causing temperatures to exceed the desired set value, which triggers alarms but does not cause injury.
Check the model number and serial numbers listed in the recall notice to see if your unit is affected. The remedy is not specified in the recall notice.
The recall states that overheating triggers alarms but does not cause injury or damage to users or materials.
We’ve drafted a message you can send K-Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0689-2025 — K-Systems K-Systems Hello, I own a K-Systems that is covered by recall Z-0689-2025 from K-Systems. 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.
