Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of BDLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 5 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list CareFusion with 28 device recalls and 4 510(k) clearances. The most recent is a 510(k) clearance dated Oct 30, 2025: BD Alaris Pump Infusion Set.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Oct 30, 2025 | BD Alaris Pump Infusion SetK250325 · FPA | 510(k) clearances |
| Oct 23, 2020 | MaxZero Extension Sets with Needle-Free Connector(s)K193088 · FPA | 510(k) clearances |
| Jul 7, 2016 | AirLife Adult Heated Wire CircuitK153234 · BZE | 510(k) clearances |
| Jan 20, 2016 | AirLife Infant Single Limb Heated Wire CircuitK151959 · BZE | 510(k) clearances |
| Nov 20, 2009 | Pyxis Anesthesia System Model 2000 (PAS 2000) Product Usage: The PAS 2000 is an anesthesia medication dispensing device that provides Class II · The recall was initiated because Carefusion has confirmed that when the PAS 2000 drawers due to inaccessability of drawe | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
