{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.", "terms": "https://open.fda.gov/terms/", "license": "https://open.fda.gov/license/", "last_updated": "2026-08-15", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "65273", "product_res_number": "Z-0126-2008", "event_date_initiated": "2007-09-11", "event_date_posted": "2008-01-03", "recall_status": "Terminated", "event_date_terminated": "2011-12-10", "res_event_number": "45328", "product_code": "GWQ", "k_numbers": [ "K021185" ], "product_description": "Viasys Healthcare NicoletOne ICU Monitor, Modular Neurodiagnostic System (containing Axiomtek Panel PC computer system), released and installed between December 2004 and March 2007 (Axiomtek Panel PC Model Number: 2147-671) VIASYS NeuroCare Part Numbers: 842-673800, 842-673900, 982A0421 and 982A0422. \nManufactured, designed, developed and marketed by VIASYS NeuroCare Inc., Madison, WI 53711", "code_info": "ON040060, ON050120, ON050130, ON050168, ON050186, ON050197, ON050199, ON050203, ON050206, ON050212, ON050220, ON050231, ON060232, ON060243, ON060254, ON060256, ON060257, ON060269, ON060270, ON060272, ON060275, ON060276, ON060277, ON060278, ON060279, ON060280, ON060288, ON060290, ON060291, ON060292, ON060299, ON070301, ON070308.", "firm_fei_number": "3010611950", "recalling_firm": "Nicolet Biomedical Div of Viasys Healthcare", "address_1": "5225 Verona Rd", "city": "Madison", "state": "WI", "postal_code": "53711-4497", "additional_info_contact": "Technical Support\n800-356-0007", "reason_for_recall": "Display lock-up: VIASYS Healthcare NicoletOne ICU Monitor freezes up during operation when using the digital video option.", "root_cause_description": "Component design/selection", "action": "Certified direct mail delivery of URGENT MEDICAL DEVICE FIELD CORRECTION (RECALL) were made to consignees on 9/11/07 by Nicolet Biomedical Div of Viasys Healthcare. The letter describes the product and problem. VIASYS requests that customers cease use of the video option of the device until the monitor can be replaced by VIASYS authorized personnel. Letter also requests consignees to fax or mail back the response form.", "product_quantity": "33", "distribution_pattern": "Worldwide Dsitribution - USA, Germany, Netherlands, Kuwait, Japan, Ireland, and China.", "openfda": { "k_number": [ "K110376", "K980214", "K923950", "K870263", "K820604", "K854663", "K231366", "K860456", "K791150", "K951507", "K023771", "K112353", "K143440", "K201819", "K991033", "K842714", "K932407", "K850418", "K053386", "K971329", "K992410", "K012079", "K802296", "K131335", "K010697", "K112107", "K925838", "K932842", "K982479", "K933951", "K002570", "K163163", "K970942", "K131383", "K180290", "K061908", "K223644", "K910972", "K180269", "K871500", "K010091", "K961642", "K842784", "K841683", "K896666", "K131266", "K901549", "K040360", "K971331", "K831324", "K113117", "K905435", "K894276", "K081151", "K930080", "K921927", "K033399", "K172271", "K864928", "K010086", "K171124", "K221963", "K042626", "K122196", "K171781", "K081741", "K822700", "K970703", "K863193", 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