{ "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": "2026-08-13", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "85318", "product_res_number": "Z-0167-2010", "event_date_initiated": "2009-07-01", "event_date_posted": "2009-11-10", "recall_status": "Terminated", "event_date_terminated": "2010-01-12", "res_event_number": "53353", "product_code": "IZI", "k_numbers": [ "K930635" ], "product_description": "Koodinat M/MP Patient Table used with Multistar Model 6239003.\n\nThe device is used as an Angiographic X-Ray System.", "code_info": "Model number 6239003. 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The firm also provided an addendum to User Manual. Direct questions about the recall to Siemens Medical Solutions USA, Inc. by calling 1-610-219-6300.", "product_quantity": "362 units", "distribution_pattern": "Nationwide Distribution.", "openfda": { "k_number": [ "K810183", "K041027", "K030139", "K842494", "K930635", "K230727", "K972229", "K181537", "K945375", "K231986", "K875374", "K914376", "K944952", "K942503", "K812238", "K100849", "K970525", "K042646", "K955519", "K915232", "K945449", "K904540", "K934496", "K033184", "K982203", "K945400", "K993765", "K853044", "K882358", "K903372", "K842495", "K133719", "K910370", "K063345", "K052039", "K973482", "K875379", "K926258", "K082907", "K922804", "K243077", "K932410", "K903371", "K911732", "K072591", "K940484", "K083745", "K933058", "K850455", "K991922", "K926082", "K903941", "K813588", "K970738", "K062360", "K974679", "K811149", "K936002", "K923112", "K875376", "K924137", "K883831", "K945540", "K060749", "K897115", "K182907", "K984545", "K234090", "K960575", "K031333", "K052076", 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