{ "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": "2026-08-20", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "175350", "product_res_number": "Z-0161-2020", "event_date_initiated": "2019-07-16", "event_date_created": "2019-10-18", "recall_status": "Open, Classified", "res_event_number": "83472", "product_code": "OCC", "k_numbers": [ "K081483", "K091667", "K112199", "K112781" ], "product_description": "xTAG Respiratory Viral Panel (RVP):\nBox Label: xTAG RVP (Respiratory Viral Panel). Catalogue Number:I019C0111\n\n in vitro diagnostic test", "code_info": "Catalogue Number:I019C0111 Device UDI: 00840487100462 Lot Numbers: IK019C-0129  IK019C-0130  IK019C-0131  IK019C-0132", "firm_fei_number": "3002777243", "recalling_firm": "Luminex Molecular Diagnostics", "address_1": "439 University Ave Suite 900 439 University Ave", "address_2": "Suite 900", "city": "Toronto", "country": "Canada", "reason_for_recall": "The Assay may give a false negative result when detecting and subtyping Influenza A (H3) and detecting RSV A in patient specimens. However, the assay will continue to detect Influenza A, Influenza B, RSV B and all other targets in accordance with each of these products performance claims.", "root_cause_description": "Device Design", "action": "An initial Customer Advisory Notice was sent to customers on Jul/16/2019 to advise customers of the firm's potential concerns of false negative results while the firm is conducting its recall investigation.\n\nOn August 8, 2019, the firm sent to customers via email an \"URGENT: MEDICAL DEVICE RECALL/FIELD CORRECTION\" Letter to customer which informed its customers of the potential concerns of false negative results and provided them with two options for handling the affected products.\n\nThe recall letter provided customers with the following options:\nOption 1:\n1. Segregate Recalled Product. Please immediately remove all affects lots from their inventory that are unused and unexpired (regardless of location) and segregate these lots in a secure location for destruction.\n\n2. Complete Acknowledgment and Receipt Form 1. Complete and return the enclosed Acknowledgment and Receipt Form 1 by email (support@luminexcorp.com) or mail (even if you do not have any product on hand), following the directions on this page and the Acknowledgment and Receipt Form. Global Support Services can assist customers in completing the form, if needed.\n\nPlease destroy the product and provide confirmation in the Acknowledgment and Receipt Form on or before July xx, 2019. The firm will replace any unused products and handle any customer concerns on a case-by-case basis. Please inform Global Support Services if you destroyed product and need a replacement(s). \n\nOption 2:\nIf customer have the affected products and wish to continue using the product for testing, customers are instructed to complete Acknowledgment and Receipt Form 2 which states that customer acknowledged that they will continue using the affected product and will not use the product for testing and reporting results for the Influenza A (H3) and RSV A.\n\nCustomers are instructed to complete and return the enclosed Acknowledgment and Receipt Form 2 by email (support@luminexcorp.com) or mail, following the directions on t", "product_quantity": "56 Kits", "distribution_pattern": "US distribution to CA, CT, MA, and PA\n\nOUS: None", "openfda": { "k_number": [ "K092566", "K181289", "K172629", "K103209", "K162331", "K152523", "K111387", "K171974", "K110764", "K132159", "K142365", "K191534", "K132129", "K083088", "K153219", "K210234", "K092500", "K193167", "K201505", "K161814", "K131584", "K152408", "K081483", "K091667", "K111775", "DEN070013", "K152386", "K120413", "K180218", "K143080", "K141931", "K161220", "K151226", "K191729", "K121942", "K113323", "K151464", "K123191", "K143653", "K160068", "K123620", "K192485", "K163636", "K093337", "K181443", "K161375", "K173932", "K131813", "K112172", "K231017", "K081030", "K232775", "K171792", "K163266", "K102170", "K183597", "K254139", "K171963", "K103776", "K170604", "K213822", "K141520", "K171552", "K110968", "K092957", "K242613", "K200065", "K112199", "K162456", "K120267", "K073029", "K153544", "K152579", "K142045", "K121003", "K103175", "K163628", "K102952", "K112781" ], "registration_number": [ "", "3021140368", "3019946577", "3002773840", "3005360469", "3005248192", "3012494290", "2024800", "3010770794", "2023365", "3006198300", "3007799234", "3004141078", "1650733", "3002777243", "3008632402", "9610126", "3006028115", "3009613136", "9681630", "3023372670", "3003018722", "3029059580", "2243471", "3016838963", "3013019728", "1528450", "3004530258", "1221359", "3038610665", "3003795116", "3010749841", "3003030793" ], "fei_number": [ "", "3021140368", "3019946577", "3005670738", "3002806559", "3002773840", "3005248192", "3012494290", "2024800", "3010770794", "2023365", "3006198300", "3007799234", "3004141078", "3002777243", "3008632402", "3006028115", "3009613136", "3023372670", "3002808845", "3003018722", "3029059580", "1000122536", "2243471", "3016838963", "3013019728", "3004530258", "1221359", "3002524000", "3038610665", "3003795116", "3010749841", "3003030793" ], "device_name": "Respiratory Virus Panel Nucleic Acid Assay System", "medical_specialty_description": "Microbiology", "regulation_number": "866.3980", "device_class": "2" } } ] }