Mckesson Technologies, Inc.
Mckesson Technologies, Inc. holds FDA 510(k) medical device clearance, cleared in 2012, with 3 FDA device recalls on record.
Top product codes for Mckesson Technologies, Inc.
FDA recalls by Mckesson Technologies, Inc.
- Z-2263-2015 — Paragon Laboratory Management
- Z-2089-2013 — 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.
- Z-1060-2014 — 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 support by communicating potential Adverse Drug Event alerts proactively during the pre-anesthesia evaluation and at the point-of-care. The system is generally indicated in the anesthetizing environment when the anesthesia provider decides to perform a patient assessment, to generate a paper and/or electronic record of the administration of anesthesia to a patient, and to document care.
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 Mckesson Technologies, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.