Carefusion Corporation
Carefusion Corporation has 3 FDA enforcement events on this register (3 product records) between 2009 and 2013: 3 device; the busiest year was 2013 with 2.
33% of its events are Class I; the most common class is Class II (2). 0 events are listed as ongoing; the recalling firm's address is in CA.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 6 Mar 2013 | Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the central programming, monitoring and power supply component for the Alaris System. | Device | Class I | 1 | Terminated |
| 6 Mar 2013 | Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the central programming, monitoring and power supply component for the Alaris System | Device | Class II | 1 | Terminated |
| 20 Nov 2009 | Pyxis Anesthesia System Model 2000 (PAS 2000) Product Usage: The PAS 2000 is an anesthesia medication dispensing device that provides medications and inventory management for the anesthesiologist at the point of care within the operating room. | Device | Class II | 1 | Terminated |
By type and class
Class I: 33% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has Carefusion Corporation had?
3 enforcement events (3 product records) on this register, 2009–2013: 3 device.
Are any Carefusion Corporation recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are Carefusion Corporation recalls?
2 Class II, 1 Class I. 33% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.