ClearanceBrief
Recall Z-0681-2016 ยท BSZ Gas-Machine, Anesthesia

GE Medical Systems, LLC

GE Healthcare, Aisys CS2,1011-9050-000; Avance Amingo,1009-9002-000, & Avance CS2, 1009-9050-000. The GE Datex-Ohmeda Aisys Anesthesia System is intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (neonatal, pediatric, adult). The device is intended for volume or pressure control ventilation. The Aisys is not suitable for use in a MRI environment.

DateJan 21, 2016 (initiated Dec 15, 2015)
StatusTerminated
ReasonThe Drive Gas Check Valve of certain Anesthesia products could become stuck in a fixed open position, which could cause pressure to build in the mechanical ventilation cycle. If this issue is left unresolved, it could result in excessive or prolonged pressure in the patient breathing circuit during ventilation potentially resulting in barotrauma.
Root causeNonconforming Material/Component
ActionGE Healthcare sent an Urgent Medical Device Correction letter dated December 15, 2015, to all affected consignees. The letter described the Safety Issue, Safety Instructions, Affected Product Details, Product Correction and Contact Information. Customers with questions were instructed to contact GE Healthcare Service at 1-800-437-1171 or their local Service Representative.
Quantity2627
DistributionWorldwide Distribution - US (nationwide including PR except NH, VT, & WY. Internationally to ALBANIA, ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, BANGLADESH, BELGIUM, BOLIVIA, BOSNIA, BRAZIL, CAMBODIA, CANADA, CHILE, CHINA, COLOMBIA, COSTA RICA, CZECH REPUBLIC, DENMARK, ECUADOR, EGYPT, ESTONIA, FINLAND
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K112722GE DATEX-OHMEDA AVANCE
Datex-Ohmeda, Inc., Dec 16, 2011
K131945GE DATEX-OHMEDA AVANCE CS2
Datex-Ohmeda, Aug 8, 2013
K132530GE DATEX-OHMEDA AISYS CS2 (AISYS CS^2)
Datex-Ohmeda, Inc., Dec 20, 2013