Z-1396-2017 Class II Terminated
FDA device recall Z-1396-2017 was initiated by Mckesson Medical Imaging on December 2, 2016 and is designated Class II. Reason for recall: Issue for customers that use an EMR login or legacy web URL login or legacy web URL login for McKesson Radiology PACS that may result in missing images in a newly imported study, and/or study imports … The recall status is terminated (terminated November 24, 2017). Affected quantity: 17.
Recall Details
- Product Type
- Devices
- Report Date
- March 8, 2017
- Initiation Date
- December 2, 2016
- Termination Date
- November 24, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 17
Product Description
McKesson Radiology 12.2 - Picture Archive Communication System (PACS)
Reason for Recall
Issue for customers that use an EMR login or legacy web URL login or legacy web URL login for McKesson Radiology PACS that may result in missing images in a newly imported study, and/or study imports that remain in an "in-progress" status.
Distribution Pattern
AK, CA, FL, HI, KY, MD, MI, MS, NH, OH, PA, TN, TX, VT
Code Information
Model 12.2