FDAFDA · Food and drugs·Recall number Z-0586-2016
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.
Published January 20, 2016 · Recall initiated: November 19, 2015
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Batteries found unresponsive after storage, not recognized by main device, and are perpetually enabled.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Thornhill Research Inc
- Distributor
- Worldwide Distribution: US distribution in state of: Virginia and to the country of: Singapore.
- Lot
- 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
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- Canada
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