Recall Z-1617-2014— Mckesson Medical Immaging
Class II · Terminated
Class II FDA medical device recall by Mckesson Medical Immaging, initiated 2014-04-17, terminated 2016-02-02. It names one FDA 510(k) clearance: K043146. Product: McKesson Radiology-PACS. McKesson Radiology is a medical image and information application that is intended to receive, transmit, store, retrieve, display, print and process digital medical images, digital medical video, and associated medical information from various medical imaging systems.. Reason: High priority alert icon was not displayed in the Study List when there are no Stat studies present. However, the High priority alert icon is visible when studies marked as Stat priority exist in the Study List..
- Recalling firm
- Mckesson Medical Immaging
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-04-17
- Terminated
- 2016-02-02
- Firm location
- Richmond, British Columbia, Canada
510(k) clearances named in this recall
1 on FDA's recordK-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.
Product description
McKesson Radiology-PACS. McKesson Radiology is a medical image and information application that is intended to receive, transmit, store, retrieve, display, print and process digital medical images, digital medical video, and associated medical information from various medical imaging systems.
Reason for recall
High priority alert icon was not displayed in the Study List when there are no Stat studies present. However, the High priority alert icon is visible when studies marked as Stat priority exist in the Study List.
Data sourced from openFDA. This site is unofficial and independent of the FDA.