McKesson Technologies, Inc.
FDA Regulatory Profile
McKesson Technologies, Inc. appears in FDA public data with 3 recalls — including 1 Class I (most serious) —, 1 510(k) clearance, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-2263-2015, Class II) was initiated on June 15, 2014. Its most recent 510(k) clearance was granted on April 20, 2012.
Summary
- Total Recalls
- 3 (1 Class I)
- 510(k) Clearances
- 1
- Inspections
- 1
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-2263-2015 | Class II | Paragon Laboratory Management | June 15, 2014 |
| Z-2089-2013 | Class II | Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense Product Usage: Automated a | July 22, 2013 |
| Z-1060-2014 | Class I | McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based | March 15, 2013 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K113633 | MCKESSON ANESTHESIA CARE | April 20, 2012 |