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All Recalls

Every Carefusion 211 Inc Dba Carefusion Recall

Sorted by most recent. Click any recall for full details.

9 recalls
CriticalFDA
Carefusion 211 Inc Dba Carefusion
Gas Delivery Engine (GDE), 16650A A continuous ventilator intended to mechanically control or assist broad spectrum patient breathing by...
Respiratory Devices·922 affected·May 17, 2016
CriticalFDA
Carefusion 211 Inc Dba Carefusion
Gas Delivery Engine (GDE)-refurbished, R16650A A continuous ventilator intended to mechanically control or assist broad spectrum patient...
Respiratory Devices·922 affected·May 17, 2016
CriticalFDA
Carefusion 211 Inc Dba Carefusion
TCA Board, 16542A A continuous ventilator intended to mechanically control or assist broad spectrum patient breathing by delivering a pr...
Respiratory Devices·922 affected·May 17, 2016
CriticalFDA
Carefusion 211 Inc Dba Carefusion
AVEA Standard with Compressor ventilator-refurbished, R17312-xx (xx = 0-14) A continuous ventilator intended to mechanically control or ...
Respiratory Devices·922 affected·May 17, 2016
CriticalFDA
Carefusion 211 Inc Dba Carefusion
AVEA Standard ventilator, 17311-xx (xx = 0 - 14) A continuous ventilator intended to mechanically control or assist broad spectrum pati...
Respiratory Devices·922 affected·May 17, 2016
CriticalFDA
Carefusion 211 Inc Dba Carefusion
AVEA GDE/UIM upgrade kit, 12283-PMN A continuous ventilator intended to mechanically control or assist broad spectrum patient breathing ...
Respiratory Devices·922 affected·May 17, 2016
CriticalFDA
Carefusion 211 Inc Dba Carefusion
Gas Delivery Engine (GDE)-1st Generation, 16222-001-99 A continuous ventilator intended to mechanically control or assist broad spectrum...
Respiratory Devices·922 affected·May 17, 2016
CriticalFDA
Carefusion 211 Inc Dba Carefusion
CareFusion AVEA ventilator, all models. Product Usage: A continuous ventilator (respirator), intended to mechanically control or assi...
Respiratory Devices·15,905 affected·Apr 3, 2015
CriticalFDA
Carefusion 211 Inc Dba Carefusion
Product Name: AVEA¿ Ventilator. All Models. The affected devices are cleared under K073069 pm 1/25/2008 and K103211 on 05/06/2011. Thi...
Respiratory Devices·19,546 affected·Sep 5, 2013