Merge Healthcare recalls

4 official recalls and safety alerts involving Merge Healthcare since 2025-03, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Merge Healthcare or the relevant agency.

  1. 2026-09-02
  2. US
    Drugs & medicalClass II

    Merge Healthcare, Inc. recalls Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation

    Software issue may cause measurements to be displayed inaccurately.

    FDA · DeviceMerge Healthcare, Inc.US Nationwide distribution in the states of California, Florida, Kentucky,…Official notice →
  3. 2026-08-12
  4. US
    Drugs & medicalClass II

    Merge Healthcare, Inc. recalls Merge PACS, medical imaging diagnostic workstation

    Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.

    FDA · DeviceMerge Healthcare, Inc.Worldwide distribution - US Nationwide and the countries of Canada, and UK.Official notice →
  5. 2025-09-10
  6. US
    Drugs & medicalClass II

    Merge Healthcare, Inc. recalls Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The Merge Hemo, Model…

    Merge Healthcare has been informed by Schiller AG (Baar, Switzerland) of an issue with the Schiller ARGUS PB-3000 Patient Data Module (PDM) where certain units trigger an error message on the Merge Hemo Client (…

    FDA · DeviceMerge Healthcare, Inc.US Nationwide distribution including in the states of Arizona, Arkansas,…Official notice →
  7. 2025-03-26
  8. US
    Drugs & medicalClass II

    Merge Healthcare, Inc. recalls VERICIS, Merge Cardio, Model/Catalog Number: Version 9.x, Software Version: 9.0.6 and 9.0.8; VERICIS is an integrated cardiovascular…

    When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements…

    FDA · DeviceMerge Healthcare, Inc.USOfficial notice →