McKesson Technologies, Inc.
McKesson Technologies, Inc. has 3 FDA enforcement events on this register (3 product records) between 2013 and 2014: 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 NC and GA.
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 |
|---|---|---|---|---|---|
| 15 Jun 2014 | Paragon Laboratory Management | Device | Class II | 1 | Terminated |
| 22 Jul 2013 | Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense Product Usage: Automated anesthesia cart that monitors and controls the dispensing of medications, narcotics and supplies during surgical procedures. | Device | Class II | 1 | Terminated |
| 15 Mar 2013 | McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects, processes,and records data both through manual entry and from monitors which themselves are attached to patients, such as in the operating room environment. The system provides clinical decision… | Device | Class I | 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 McKesson Technologies, Inc. had?
3 enforcement events (3 product records) on this register, 2013–2014: 3 device.
Are any McKesson Technologies, Inc. recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are McKesson Technologies, Inc. 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.