FDA Medical Device Recalls (openFDA)
Thornhill Research Inc: MOVES System, an emergency ventilator with suction, oxygen concentrator and multi-parameter patient monitoring capabilities. The 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.
- Recall number
- Z-0586-2016
- Recalling firm
- Thornhill Research Inc
- Product
- MOVES System, an emergency ventilator with suction, oxygen concentrator and multi-parameter patient monitoring capabilities. The 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.
- Status
- Terminated
- Initiated
- 2015-11-19
- Posted
- 2016-01-11
- Terminated
- 2019-04-12
- Reason
- Batteries found unresponsive after storage, not recognized by main device, and are perpetually enabled.
- Root cause
- 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. For questions customers were instructed to call 416-597-1325.
- Quantity
- 83 units
- Distribution
- Worldwide Distribution: US distribution in state of: Virginia and to the country of: Singapore.
- Lot, serial or model codes
- 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
- 510(k) numbers
- ["K093261"]
- PMA numbers
- not on file
- Product code
- BTL
- Firm FEI
- 3005803793
- Firm city
- Toronto
- Firm state
- not on file
- Firm country
- Canada
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28