{ "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": "142381", "product_res_number": "Z-0586-2016", "event_date_initiated": "2015-11-19", "event_date_posted": "2016-01-11", "recall_status": "Terminated", "event_date_terminated": "2019-04-12", "res_event_number": "72867", "product_code": "BTL", "k_numbers": [ "K093261" ], "product_description": "MOVES System, an emergency ventilator with suction, oxygen concentrator and multi-parameter patient monitoring capabilities.\n\nThe MOVES System is a portable computer controlled electrically powered transport emergency ventilator intended to provide continuous or intermittent ventilatory support for the care of adults who require ventilation.", "code_info": "MS201205001, MS201205002, MS201205003, MS201205004, MS201205005, MS201212001, MS201212002, MS201212003, MS201212004, MS201212005, MS201212006, MS201212007, MS201212008, MS201212009, MS201212010, MS201212011, MS201212012, MS201212013, MS201212024, MS201212025, MS201212026, MS201212028, MS201212029, MS201212030, MS201212031, MS201212032, MS201212033, MS201212034, MS201212035, MS201212036, MS201212037, MS201212038, MS201212039, MS201212040, MS201212041, MS201212042, MS201212053, MS201212054, MS201212055, MS201212056, MS201212057, MS201212058, MS201212059, MS201212060, MS201212061, MS201212062, MS201212062, MS201212063, MS201212064, MS201212065, MS201212066, MS201212067, MS201212068, MS201212069, MS201212070, MS201212014, MS201212015, MS201212016, MS201212017, MS201212018, MS201212019, MS201212020, MS201212021, MS201212022, MS201212023, MS201212043, MS201212044, MS201212045, MS201212046, MS201212047, MS201212048, MS201212049, MS201212050, MS201212051, MS201212052, MS201212071, MS201212072, MS201212073, MS201212074, MS201212075, MS201212076, MS201212077, MS201212078, MS201212079", "firm_fei_number": "3005803793", "recalling_firm": "Thornhill Research Inc", "address_1": "210 Dundas St W Suite 200 210 Dundas St W", "address_2": "Suite 200", "city": "Toronto", "country": "Canada", "additional_info_contact": "Kipton Lade\n1-416-597-1325", "reason_for_recall": "Batteries found unresponsive after storage, not recognized by main device, and are perpetually enabled.", "root_cause_description": "Component design/selection", "action": "Thornhill Research sent a Recall Notification letter dated December 15, 2015 to affected customers. The letter identified the affected products, problem and actions to be taken. Customers were instructed to update their device software.\n\nFor questions customers were instructed to call 416-597-1325.", "product_quantity": "83 units", "distribution_pattern": "Worldwide Distribution: US distribution in state of: Virginia and to the country of: Singapore.", "openfda": { "k_number": [ "K123957", "K093913", "K051889", "K092085", "K093261", "K021520", "K070120", "K862192", "K932170", "K140707", "K882833", "K080692", "K910201", "K861272", "K221634", "K182956", "K941870", "K073261", "K913039", "K983785", "K030803", "K991785", "K142096", "K051476", "K780168", "K020899", "K874656", "K911261", "K870424", "K070210", "K173373", "K001430", "K021841", "K944349", "K070636", "K863410", "K051469", "K083507", "K102542", "K043495", "K041473", "K860077", "K991195", "K080063", "K921926", "K910434", "K910435", "K951126", "K792453", "K141595", "K242769", "K193191", "K800456", "K853971", "K830404", "K202219", "K983643", "K901846", "K093862", "K862830", "K941871", "K083385", "K051322", "K924272", "K855092", "K161420", "K132759", "K932200", "K072214", "K132021", "K140049", "K915564", "K983857", "K071527", "K090356", "K920910", "K904920", "K032386", "K884089", "K905697", "K892885", "K131098", "K931473", "K973975", "K841893", "K895946", "K112783", "K982225", "K131877", "K040090", "K960515", "K071221", "K944397", "K162968", "K932199", "K771299", "K983705", "K081330", "K851337", "K910699" ], "device_name": "Ventilator, Emergency, Powered (Resuscitator)", "medical_specialty_description": "Anesthesiology", "regulation_number": "868.5925", "device_class": "2", "registration_number": [ "3030733800", "", "3009746061", "3020460367", "3014220748", "3015997711", "9681209", "9610861", "3011237704", "3031754300", "3008258694", "3025434453", "3012104670", "3020476987", "3017365972", "3005783425", "3003697063", "2951529", "2134752", "8043316", "3005652389", "3005998497", "1526863", "3012542015", "1823393", "3009884346", "3024290085", "2518436", "9616567", "3005803793", "2025816", "1625392", "3008729547", "8044169", "3044994756", "3007734888", "1314417", "3006783791", "3036470679", "1024404", "3008342612", "9611500", "3013557562", "9611451", "1924066", "2022648", "2085602" ], "fei_number": [ "3030733800", "", "3009746061", "3020460367", "3014220748", "3015997711", "3002628192", "3011237704", "3001104093", "3031754300", "3008258694", "3025434453", "3012104670", "3020476987", "3017365972", "3005783425", "1000307109", "3003697063", "1526863", "3005998497", "3012542015", "1823393", "3009884346", "3024290085", "2518436", "3004846435", "3005803793", "2025816", "3002963732", "3008729547", "3003319165", "3044994756", "3007734888", "1314417", "3000210616", "3006783791", "3036470679", "1024404", "3008342612", "1000283452", "3002806988", "3013557562", "1924066", "3003007822", "2022648", "1000058335", "3002807836" ] } } ] }