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CareFusion 203 recalls

CareFusion 203 has 2 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 1 Oct 2014.

Total recalls2since 2012

Last 12 months0reported

Class I2100% of total

Ongoing0latest 1 Oct 2014

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 2 100%Class II 0 0%Class III 0 0%

Why carefusion 203 is recalled

Other Reasons150%
Device Malfunction150%

Product types

CPAP & Ventilators2100%

By year

2014150%
2012150%

All carefusion 203 recalls, newest first

2 total

Reported	Class	Recall	Company	Reason	Where
1 Oct 2014Device	CLASS I	CareFusion EnVe and ReVel Ventilators recalled by CareFusion 203	CareFusion 203	Other	Nationwide
25 Jul 2012Device	CLASS I	CareFusion EnVe Ventilator Designed recalled by CareFusion 203	CareFusion 203	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.