--- title: "Brand Name: K-Systems Product Name: T47 Warming Plate Model/Catalog Number: K... — FDA record Z-0690-2025 | Is It on Recall" description: "The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value," url: https://isitonrecall.com/recall/fda-device-z-0690-2025-brand-name-k-systems-product-name-t47-warming-plate-model-catalog-number-k23055-software-version-n-a/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # Brand Name: K-Systems Product Name: T47 Warming Plate Model/Catalog Number: K23055 Software Version: N/A Product Desc... — FDA record Z-0690-2025 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date Nov 15, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: Brand Name: K-Systems Product Name: T47 Warming Plate Model/Catalog Number: K23055 Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g., gametes and embryos), at closely regulated and monitored temperatures, during assisted reproduction examination and processing procedures. It may support a more comprehensive growth environment [e.g., temperature, carbon dioxide (CO2) and oxygen (O2) concentration]; it typically has adjustment and monitoring controls. Component: No - **Reason**: 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. - **Classification**: Class II - **Recalling firm**: CooperSurgical, Inc. - **Quantity**: 35 units - **Agency-reported status**: Ongoing - **Source record identifier**: Z-0690-2025 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0690-2025%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | Version or Model: K23055; Primary DI Number: 00888937025064; Serial Numbers: 2223KH01 , 2223KH02 , 2223KH03 , 2223KH04 , 2223KH05 , 2223KH06 , 2223KH07 , 2223KH08 , 2223KH09 , 2223KH10 , 2235KH21 , 2235KH22 , 2235KH23 , 2235KH24 , 2235KH25 , 2235KH26 , 2235KH27 , 2235KH28 , 2235KH29 , 2235KH30 , 2237KH01 , 2237KH02 , 2237KH03 , 2237KH04 , 2237KH05 , 2237KH06 , 2237KH07 , 2237KH08 , 2237KH09 , 2237KH10 , 2250KH11 , 2250KH12 , 2250KH13 , 2250KH14 , 2250KH15 , 2250KH16 , 2250KH17 , 2250KH18 , 2250KH19 , 2250KH20 , 2303KH41 , 2303KH42 , 2303KH43 , 2303KH44 , 2303KH45 , 2303KH46 , 2303KH47 , 2303KH48 , 2303KH49 , 2303KH50 , 2309KH31 , 2309KH32 , 2309KH33 , 2309KH34 , 2309KH35 , 2309KH36 , 2309KH37 , 2309KH38 , 2309KH39 , 2309KH40 , 2311KH16 , 2311KH17 , 2311KH18 , 2311KH19 , 2311KH20 , 2311KH21 , 2311KH22 , 2311KH23 , 2311KH24 , 2311KH25 , 2320KH41 , 2320KH42 , 2320KH43 , 2320KH44 , 2320KH45 , 2320KH46 , 2320KH47 , 2320KH48 , 2320KH49 , 2320KH50 , 2324KH33 , 2324KH34 , 2324KH35 , 2324KH36 , 2324KH37 , 2324KH38 , 2324KH39 , 2324KH40 , 2324KH41 , 2324KH42 , 2327KH20 , 2327KH21 , 2327KH22 , 2327KH23 , 2327KH24 , 2327KH25 , 2327KH26 , 2327KH27 , 2327KH28 , 2327KH29 , 2333KH01, 2333KH02, 2333KH03, 2333KH04, 2333KH05, 2333KH06, 2333KH07, 2333KH08, 2333KH09, 2333KH10, 2333KH21, 2333KH22, 2333KH23, 2333KH24, 2333KH25, 2333KH26, 2333KH27, 2333KH28, 2333KH29, 2333KH30, 2333KH31, 2333KH32, 2333KH33, 2333KH34, 2333KH35, 2335KH51, 2335KH52, 2335KH53, 2335KH54, 2335KH55, 2335KH56, 2335KH57, 2335KH58, 2335KH59, 2335KH60, 2335KH61, 2335KH62, 2335KH63, 2335KH64, 2335KH65, 2335KH66, 2335KH67, 2335KH68, 2335KH69, 2335KH70, 2335KH71, 2335KH72, 2335KH73, 2335KH74, 2335KH75, 2335KH76, 2335KH77, 2335KH78, 2335KH79, 2335KH80, 2335KH81, 2335KH82, 2335KH83, 2335KH84, 2335KH85, 2335KH86, 2335KH87, 2335KH88, 2335KH89, 2335KH90, 2345KH11, 2345KH12, 2345KH13, 2345KH14, 2345KH15, 2345KH16, 2345KH17, 2345KH18, 2345KH19, 2345KH20, 2345KH21, 2345KH22, 2345KH23, 2345KH24, 2345KH25, | Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution States: NC, NJ, TX, VA, IL, NY, CA, PA Please note: The countries below, excluding Iraq, all consider these devices to be "lab equipment", not medical devices and are not subject to classification or recall guidelines. Countries: AT, AU, BE, BH, BR, CA, CH, CN, CZ, DE, EG, ES, ET, FR, GB, GH, HU, ID, IE, IL, IN, IQ, IT, JO, JP, KR, KW, LB, MA, MK, MT, NL, NO, PE, PH, PK, PT, QA, RO, RS, SA, SD, SE, SO,TR, TW, TZ, US, ZA States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address. - [California](https://isitonrecall.com/state/california/) - [Delaware](https://isitonrecall.com/state/delaware/) - [Idaho](https://isitonrecall.com/state/idaho/) - [Illinois](https://isitonrecall.com/state/illinois/) - [Indiana](https://isitonrecall.com/state/indiana/) - [Massachusetts](https://isitonrecall.com/state/massachusetts/) - [Montana](https://isitonrecall.com/state/montana/) - [North Carolina](https://isitonrecall.com/state/north-carolina/) - [New Jersey](https://isitonrecall.com/state/new-jersey/) - [New York](https://isitonrecall.com/state/new-york/) - [Pennsylvania](https://isitonrecall.com/state/pennsylvania/) - [South Dakota](https://isitonrecall.com/state/south-dakota/) - [Texas](https://isitonrecall.com/state/texas/) - [Virginia](https://isitonrecall.com/state/virginia/) ## Dates in the source - **Report date**: Dec 25, 2024 - **Recall initiation date**: Nov 15, 2024 - **Center classification date**: Dec 18, 2024 FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0690-2025%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [CooperSurgical, Inc. records](https://isitonrecall.com/brand/coopersurgical-inc/)