Merge PACS 7.2Recalls & reported problems
Merge Healthcare Solutions Inc. · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842000100409), received between Sep 30, 2020 and Sep 30, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Missing Test Results” (1 report).
13 other recalls cover devices cleared under the same FDA submission (K082144); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Missing Test Results1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2020Missing Test Results; Missing Test Results
MERGE PACS IS A STANDARDS-BASED MEDICAL IMAGING DIAGNOSTIC WORKSTATION THAT SERVES AS AN ADJUNCT TO ASSIST THE CLINICIAN TO VIEW, READ, AND REPORT THEIR FINDINGS. MERGE PACS PROCESSES AND DISPLAYS MEDICAL IMAGES FROM DICOM-COMPLIANT MODALITIES. THE DEVICE IS DESIGNED TO ENABLE EFFICIENT WORKFLOWS BY MAINTAINING CLINICIANS' WORKLISTS AND RETRIEVING AND MANAGING STUDIES FOR READING, REPORTING, COMMUNICATION, AND STORAGE. MERGE PACS SOFTWARE RUNS ON OFF-THE-SHELF COMPUTER HARDWARE AND CAN BE CONFIGURED TO OPERATE STANDALONE OR TO INTEGRATE WITH VENDOR-NEUTRAL IMAGING ARCHIVES (VNAS), SUCH AS ICONNECT ENTERPRISE ARCHIVE (ICEA) FOR IMAGE STORAGE, AND WITH RADIOLOGICAL AND HOSPITAL INFORMATION SYSTEMS (RIS AND HIS) AND MEDICAL RECORD SYSTEMS (EMR, EHR, ETC.). ON (B)(6) 2020, A CUSTOMER CONTACTED MERGE HEALTHCARE TO REPORT THAT SOME IMAGES IN A MAMMOGRAPHY SERIES WERE NOT DISPLAYING AND WERE MISSED OR SKIPPED. MERGE HEALTHCARE SUPPORT IS CURRENTLY IN THE PROCESS OF ENGAGING THE CUSTOMER TO DETERMINE THE ISSUE AND NEXT STEPS. WHEN FURTHER INFORMATION BECOMES AVAILABLE, A SUPPLEMENTAL REPORT WILL BE FILED. BASED ON THIS, THERE IS A POTENTIAL FOR DELAY IN TREATMENT THAT COULD CAUSE HARM TO T
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10609388 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K082144. One submission often covers many models, so check the product and lot details in each record.
- Z-2601-2017 · May 24, 2017 · TerminatedMerge OrthoPACS software. The firm name on the label is Merge Healthcare, Hartland, WI.
- Z-2591-2017 · May 8, 2017 · TerminatedMerge PACS software. Merge PACS (Picture Archiving Communication System) is designed and marketed for soft copy reading, communication, and storage of studies produced by digital
- Z-2590-2017 · May 8, 2017 · TerminatedMerge PACS software. The firm name on the label is Merge Healthcare, Hartland, WI.
- Z-1431-2017 · Apr 4, 2016 · TerminatedMerge PACS software. The firm name on the label is Merge Healthcare.
- Z-1176-2017 · Apr 4, 2016 · TerminatedMerge PACS software. The firm name on the label is Merge Healthcare, Hartland, WI.
- Z-0726-2017 · Mar 28, 2016 · TerminatedMerge PACS software. Merge PACS (Picture Archiving Communication System) is designed and marketed for soft copy reading, communication and storage of studies produced by digital
- Z-0599-2017 · Mar 28, 2016 · TerminatedMerge PACS software. Product Usage: Merge PACS (Picture Archiving Communication System) is designed and marketed for soft copy reading, communication and storage of studies prod
- Z-2363-2016 · Feb 5, 2016 · TerminatedMerge PACS software. The firm name on the label is Merge Healthcare, Inc., Hartland, WI. Intended to create and display two-dimensional and three-dimensional images of anatomy fr
- Z-2531-2016 · Jan 30, 2016 · TerminatediConnect Access used with Merge PACS software provides medical specialists with access to diagnostic quality images, reports, and various types of patient data over conventional TC
- Z-2301-2016 · Jan 30, 2016 · TerminatedMerge PACS software. The firm name on the label is Merge Healthcare, Hartland, WI. Intended to create and display two-dimensional and three-dimensional images of anatomy from a
- Z-2532-2016 · Jan 30, 2016 · TerminatediConnect Access used with Ortho PACS software provides medical specialists with access to diagnostic quality images, reports, and various types of patient data over conventional TC
- Z-2303-2016 · Jan 30, 2016 · TerminatedMerge PACS software. The firm name on the label is Merge Healthcare, Hartland, Wisconsin. Merge PACS 6.0 is software intended to create and display two-dimensional and three-dime
- Z-2379-2016 · Jan 30, 2016 · TerminatedMerge PACS software. Product was distributed under the AMICAS label, Brighton, MA, but labeling was later changed to Merge Healthcare, Hartland, WI.
Other System, Image Processing, Radiological devices
- Interventional Workspot Interventional Workspot - 1Philips Medical Systems Nederland B.V. · System, Image Processing, Radiological13 recalls24 reports
- Synapse Radiology PACS Synapse Radiology PACS Software LicenseFujifilm Healthcare Americas Corporation · System, image processing, radiological9 recalls38 reports
- CENTRICITY UNIVERSAL VIEWER ZFP CLIENT 6.0Ge Healthcare · System, image processing, radiological8 recalls0 reports
- CENTRICITY UNIVERSAL VIEWER 6.0Ge Healthcare · System, image processing, radiological8 recalls0 reports
- CENTRICITY UNIVERSAL VIEWER 7.0Ge Healthcare · System, image processing, radiological6 recalls0 reports
- IntelliSpace Cardiovascular 8Philips Medical Systems Nederland B.V. · System, Image Processing, Radiological2 recalls132 reports
- CA1000 2.0 SP 14Ge Healthcare · System, image processing, radiological4 recalls0 reports
- VMA 2Ortho Kinematics, Inc. · System, Image Processing, Radiological4 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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