CooperSurgical recalls K-Systems G85 Mini Incubators with model K22074 that may overheat during assisted reproduction procedures, causing potential temperature control issues.
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 G85 Mini Incubators with model K22074 due to possible overheating. This could lead to incorrect temperature settings during sensitive reproductive procedures, though the device alarms when temperatures exceed the set point.
The incubator may overheat, causing temperatures to exceed the desired set point. While the device alarms when this happens, the risk of incorrect temperature settings could affect delicate reproductive procedures.
Reproductive specialists and clinics using K-Systems G85 Mini Incubators with model K22074 for assisted reproductive procedures. Those handling embryos or gametes are most at risk from temperature fluctuations.
Check for model number K22074 on the incubator. The serial numbers listed include 2244KH01 through 2321KH20. This product was sold for assisted reproductive procedures.
Monitor the incubator for alarms indicating overheating, as the device will alert when temperatures exceed the set point.
The incubator has a safety feature that alarms when temperatures exceed the set point, but it may overheat during use.
The device will alarm when temperatures exceed the set point, but the recall does not specify a specific action for this scenario.
Check for model number K22074 on the incubator. The serial numbers listed include 2244KH01 through 2321KH20.
We’ve drafted a message you can send K-Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0688-2025 — K-Systems K-Systems Hello, I own a K-Systems that is covered by recall Z-0688-2025 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.
