{ "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": "2026-09-17", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "195990", "product_res_number": "Z-1786-2022", "event_date_initiated": "2022-08-31", "event_date_posted": "2022-09-23", "recall_status": "Open, Classified", "res_event_number": "90839", "product_code": "IZL", "k_numbers": [ "K211423" ], "product_description": "MICRO-X ROVER MOBILE X-RAY SYSTEM, MXU-RV19", "code_info": "Model Number: MXU-RV19\nUDI Codes:\n(01)09357123000013(11)210326(21)00222\n(01)09357123000013(11)210628(21)00234\n(01)09357123000013(11)210629(21)00235\n(01)09357123000013(11)210629(21)00236\n(01)09357123000013(11)210630(21)00237\n(01)09357123000013(11)210708(21)00238\n(01)09357123000013(11)210721(21)00240\n(01)09357123000013(11)210910(21)00261\n(01)09357123000013(11)210913(21)00262\n(01)09357123000013(11)210914(21)00263\n(01)09357123000013(11)210921(21)00264\n(01)09357123000013(11)210922(21)00265\n(01)09357123000013(11)210923(21)00266\n(01)09357123000013(11)210927(21)00267\n(01)09357123000013(11)211006(21)00268\n(01)09357123000013(11)211008(21)00269\n(01)09357123000013(11)211011(21)00270\n(01)09357123000013(11)211011(21)00271\n(01)09357123000013(11)211012(21)00272\n(01)09357123000013(11)211013(21)00273\n(01)09357123000013(11)211013(21)00274\n(01)09357123000013(11)211210(21)00288\n(01)09357123000013(11)211213(21)00289\n(01)09357123000013(11)211213(21)00290\n(01)09357123000013(11)220329(21)00305\n(01)09357123000013(11)220330(21)00306\n(01)09357123000013(11)220331(21)00307\n(01)09357123000013(11)220401(21)00308\n(01)09357123000013(11)220404(21)00309\n(01)09357123000013(11)220405(21)00310\n(01)09357123000013(11)220406(21)00311\n(01)09357123000013(11)220404(21)00312\n\nSerial Numbers:\n222\n234\n235\n236\n237\n238\n240\n261\n262\n263\n264\n265\n266\n267\n268\n269\n270\n271\n272\n273\n274\n288\n289\n290\n305\n306\n307\n308\n309\n310\n311\n312", "firm_fei_number": "3012855798", "recalling_firm": "Micro-X Ltd.", "address_1": "A14 6 MAB Eastern Promenade 6 MAB Eastern Promenade", "city": "Tonsley", "country": "Australia", "reason_for_recall": "Software calibration error with product equip with a Dose Area Product (DAP) meter. This results in the product displaying the incorrect DAP meter values which may impede radiation exposure management decisions", "root_cause_description": "Process control", "action": "On or about 09/31/2022, the firm sent an \"URGENT: MEDICAL DEVICE CORRECTION\" Letter via email/telephone to customers informing them that during an internal data analysis on 08/18/2022, Micro-X Ltd identified software calibration errors with the product equipped with a Dose Area Product (DAP) meter. This resulted in the product displaying incorrect DAP meter values. The DICOM image produced by the system will report a DAP measurement in microgray/square meter that is 8 to 10 times lower than the actual dose delivered.\n\nCustomers are instructed to:\n1. Inspect their stock immediately and place the Recall Notification Letter on the affected product and quarantine affected product on hand to prevent further use.\n2. Contact the nominated Service representative to arrange the re-calibration of the DAP Meter. Email: support-us@micro-x.com or Phone 1-206-249-8764.\n3.Previous version of Service Documentation (ROV208-2 Acceptance and Compliance Testing Instructions) which includes inaccurate DAP calibration processes are to be removed from use.\n4. Complete and return Acknowledgement and Receipt Form immediately to Micro-X LTD in Australia: support@micro-x.com and copy djerkovic@micro-x.com\n5. Ensure relevant staff members are informed of the Recall and if affected units have been supplied/transferred to another facility, inform them immediately.\n\nFor question or further assistance, contact Regulatory Affairs Manager at djerkovic@micro-x.com", "product_quantity": "42 units", "distribution_pattern": "Worldwide distribution - U.S. Nationwide distribution in the states of CA, NV, NY, OH, TX and WA and the countries of Australia, France, Israel, Japan, and United Arab Emirates.", "openfda": { "k_number": [ "K182234", "K141895", "K894643", "K173187", "K253058", "K111912", "K222353", "K210982", "K100400", "K250750", "K931279", "K230581", "K170755", "K200726", "K244049", "K042361", "K191813", "K241505", "K162687", "K930049", "K041763", "K183292", "K042866", "K080945", "K061685", "K222896", "K203782", "K202353", "K052897", "K242515", "K173602", "K972365", "K932354", "K221417", "K211423", "K072392", "K781676", "K862452", "K122697", "K260085", "K022337", "K142492", "K153059", 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