Carefusion 211 recalls

Carefusion 211 has 12 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 22 Jun 2016. The most frequent reason is device malfunction.

Total recalls12since 2016

Last 12 months0reported

Class I12100% of total

Ongoing0latest 22 Jun 2016

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 12 100%Class II 0 0%Class III 0 0%

Why carefusion 211 is recalled

Device Malfunction12100%

Product types

CPAP & Ventilators12100%

By year

201612100%

All carefusion 211 recalls, newest first

12 total

Reported	Class	Recall	Company	Reason	Where
22 Jun 2016Device	CLASS I	AVEA Comprehensive ventilator-refurbished, R17310-xx recalled	Carefusion 211	Device Malfunction	Nationwide
22 Jun 2016Device	CLASS I	AVEA Comprehensive ventilator, 17310-xx (xx = recalled by Carefusion 211	Carefusion 211	Device Malfunction	Nationwide
22 Jun 2016Device	CLASS I	AVEA Standard ventilator-refurbished, R17311-xx recalled	Carefusion 211	Device Malfunction	Nationwide
22 Jun 2016Device	CLASS I	AVEA GDE upgrade kit, 12284-PMN A continuous ventilator recalled	Carefusion 211	Device Malfunction	Nationwide
22 Jun 2016Device	CLASS I	AVEA Standard with Compressor ventilator, 17312-xx (xx = recalled	Carefusion 211	Device Malfunction	Nationwide
22 Jun 2016Device	CLASS I	Gas Delivery Engine (GDE)-1st Generation recalled by Carefusion 211	Carefusion 211	Device Malfunction	Nationwide
22 Jun 2016Device	CLASS I	AVEA GDE/UIM upgrade kit, 12283-PMN A continuous ventilator recalled	Carefusion 211	Device Malfunction	Nationwide
22 Jun 2016Device	CLASS I	AVEA Standard ventilator, 17311-xx (xx = recalled by Carefusion 211	Carefusion 211	Device Malfunction	Nationwide
22 Jun 2016Device	CLASS I	AVEA Standard with Compressor ventilator-refurbished recalled	Carefusion 211	Device Malfunction	Nationwide
22 Jun 2016Device	CLASS I	TCA Board, 16542A A continuous ventilator intended to recalled	Carefusion 211	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.