Carefusion 2200, Inc.

Carefusion 2200, Inc. holds 12 FDA 510(k) medical device clearances, first cleared 2011, most recent 2021, with 110 FDA device recalls on record.

Top product codes for Carefusion 2200, Inc.

FDA recalls by Carefusion 2200, Inc.

10 most recent of 110

Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.

Recent clearances by Carefusion 2200, Inc.

Data sourced from openFDA. This site is unofficial and independent of the FDA.