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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls
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Z-0687-2025 - Brand Name: K-Systems Product Name: G73 Dry Bath Incubator Model/Catalog Number: K22065 Product Description: An electrically-powered device intended to provide suitable warming and/or incubation co... 2 12/18/2024 FEI # 1216677
CooperSurgical, Inc.
Z-0688-2025 - Brand Name: K-Systems Product Name: G85 Mini Incubator Model/Catalog Number: K22074 Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming a... 2 12/18/2024 FEI # 1216677
CooperSurgical, Inc.
Z-0692-2025 - Brand Name: K-Systems Product Name: Multiple/unknown Model/Catalog Number: Multiple/unknown Software Version: N/A Product Description: An electrically-powered device intended to provide suitable w... 2 12/18/2024 FEI # 1216677
CooperSurgical, Inc.
Z-0690-2025 - 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 an... 2 12/18/2024 FEI # 1216677
CooperSurgical, Inc.
Z-0691-2025 - Brand Name: K-Systems Product Name: R65 Trolley Model/Catalog Number: K24012 Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming and/or i... 2 12/18/2024 FEI # 1216677
CooperSurgical, Inc.
Z-0689-2025 - Brand Name: K-Systems Product Name: T47 Warming Plate Model/Catalog Number: K23054 Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming an... 2 12/18/2024 FEI # 1216677
CooperSurgical, Inc.
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