CooperSurgical recalls K-Systems G73 Dry Bath Incubators (model K22065) due to potential overheating. The incubator may exceed set temperatures, triggering alarms but risking improper temperature control for reproductive materials.
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 is recalling K-Systems G73 Dry Bath Incubators with model number K22065 because they may overheat and exceed the set temperature. This could lead to improper temperature control for reproductive biological materials like embryos during assisted reproduction procedures.
The incubator's warming surfaces or well temperatures may exceed the desired set temperature, causing improper temperature control for reproductive biological materials. The device will alarm when temperatures get too high, but the risk of overheating could still occur if the alarm is not addressed.
Users of K-Systems G73 Dry Bath Incubators with model K22065, primarily fertility clinics and laboratories handling reproductive biological materials. Individuals using these incubators for assisted reproduction procedures are most at risk.
Check for model number K22065 on the incubator. Serial numbers listed include 2202KH46 through 2332KH20. These units were sold with the specific model number and serial numbers provided.
If the incubator alarms for overheating, stop using it immediately and contact CooperSurgical for further instructions.
Confirm the model number is K22065 to determine if your incubator is affected.
The incubator may overheat and exceed the set temperature, which could lead to improper temperature control for reproductive biological materials like embryos during assisted reproduction procedures.
Stop using it immediately and contact CooperSurgical for further instructions.
Check for model number K22065 and serial numbers listed in the recall notice (2202KH46 through 2332KH20).
We’ve drafted a message you can send K-Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0687-2025 — K-Systems K-Systems Hello, I own a K-Systems that is covered by recall Z-0687-2025 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.
