Recall Z-1728-2014— Mckesson Medical Immaging
Class II · Terminated
Class II FDA medical device recall by Mckesson Medical Immaging, initiated 2014-05-29, terminated 2017-03-31. It names one FDA 510(k) clearance: K043146. Product: Horizon Medical Imaging Horizon Medical Imaging is a medical image and information management 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: Firm received a complaint that an unreported study performed that day could not be opened from the archive..
- Recalling firm
- Mckesson Medical Immaging
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-05-29
- Terminated
- 2017-03-31
- 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
Horizon Medical Imaging Horizon Medical Imaging is a medical image and information management 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
Firm received a complaint that an unreported study performed that day could not be opened from the archive.
Data sourced from openFDA. This site is unofficial and independent of the FDA.