This page has been archived on the Web
Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.
Merge PACS
- Starting date:
- August 26, 2016
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-60240
Affected Products
Merge PACS
Reason
This recall has been initiated because studies that have QC or PDE or HL7 ADT updates applied may fail to propagate via TelMed protocol to the designation server and may fail to import on the destination server. Use of this product may result in demographic changes to studies not being passed downstream to other PACS servers whether in-house or used for tele radiology transfers.
Affected products
Merge PACS
Lot or serial number
6.6.1
6.6.1.1
6.6.2
6.6.2.1
6.6.2.2
7.0
7.0.1
Model or catalog number
MERGE PACS
Companies
- Manufacturer
-
Merge Healthcare Incorporated,
900 Walnut Ridge Drive,
Hartland
53029
Wisconsin
UNITED STATES