---
title: "Merge Healthcare, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search Merge Healthcare, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/merge-healthcare-inc/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# Merge Healthcare, Inc. recall records

**9** reported ongoing

9 records in this archive. Latest source date Jul 22, 2026.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## Records and reported status

Jul 22, 2026 FDA device enforcement

### [Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation](https://isitonrecall.com/recall/fda-device-z-3004-2026-merge-pacs-and-merge-orthopacs-medical-imaging-diagnostic-workstation/)

Software issue may cause measurements to be displayed inaccurately.

Class II Reported ongoing

Distribution: US Nationwide distribution in the states of California, Florida, Kentucky, Nebraska, Washington.

[Official source for Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3004-2026%22)

Jun 30, 2026 FDA device enforcement

### [Merge PACS, medical imaging diagnostic workstation](https://isitonrecall.com/recall/fda-device-z-2874-2026-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.

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, and UK.

[Official source for Merge PACS, medical imaging diagnostic workstation](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2874-2026%22)

Jun 30, 2026 FDA device enforcement

### [Merge OrthoPACS, medical imaging diagnostic workstation](https://isitonrecall.com/recall/fda-device-z-2875-2026-merge-orthopacs-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.

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, and UK.

[Official source for Merge OrthoPACS, medical imaging diagnostic workstation](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2875-2026%22)

Aug 11, 2025 FDA device enforcement

### [Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The Merge Hemo, Model RCSV2 device is a hemodynamics recording ...](https://isitonrecall.com/recall/fda-device-z-2518-2025-merge-hemo-model-rcsv2-model-catalog-number-99-01172-00-software-versions-11-1-and-11-1-1-product-de/)

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 (Pressure Sensor Defective) during non-invasi...

Class II Reported ongoing

Distribution: US Nationwide distribution including in the states of Arizona, Arkansas, California, Florida, Louisiana, Mississippi, North Carolina, North Dakota, Oklahoma, Pennsylvania, Georg...

[Official source for Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Prod...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2518-2025%22)

Feb 19, 2025 FDA device enforcement

### [VERICIS, Merge Cardio, Model/Catalog Number: Version 9.x, Software Version: 9.0.6 and 9.0.8; VERICIS is an integrated cardiovascular information system classified as a picture a...](https://isitonrecall.com/recall/fda-device-z-1398-2025-vericis-merge-cardio-model-catalog-number-version-9-x-software-version-9-0-6-and-9-0-8-vericis-is-an/)

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 may be inconsistent with the associated p...

Class II Reported ongoing

Distribution: US

[Official source for VERICIS, Merge Cardio, Model/Catalog Number: Version 9.x, Software Version: 9.0.6 and 9.0.8; VERI...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1398-2025%22)

Feb 19, 2025 FDA device enforcement

### [VERICIS, Merge Cardio, Model/Catalog Number: Version 10.x, Software Version: 10.0, 10.1.1.1, 10.1.2, 10.2.0, 10.2 P2 , 10.3; The VERICIS is an integrated cardiovascular informat...](https://isitonrecall.com/recall/fda-device-z-1399-2025-vericis-merge-cardio-model-catalog-number-version-10-x-software-version-10-0-10-1-1-1-10-1-2-10-2-0/)

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 may be inconsistent with the associated p...

Class II Reported ongoing

Distribution: US

[Official source for VERICIS, Merge Cardio, Model/Catalog Number: Version 10.x, Software Version: 10.0, 10.1.1.1, 10.1...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1399-2025%22)

Feb 19, 2025 FDA device enforcement

### [VERICIS, Merge Cardio, Model/Catalog Number: Version 11.x, Software Version: 11.0.2, 11.0.3, 11.0.4, 11.1, 11.1.1; The VERICIS is an integrated cardiovascular information system...](https://isitonrecall.com/recall/fda-device-z-1400-2025-vericis-merge-cardio-model-catalog-number-version-11-x-software-version-11-0-2-11-0-3-11-0-4-11-1-11/)

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 may be inconsistent with the associated p...

Class II Reported ongoing

Distribution: US

[Official source for VERICIS, Merge Cardio, Model/Catalog Number: Version 11.x, Software Version: 11.0.2, 11.0.3, 11.0...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1400-2025%22)

Feb 19, 2025 FDA device enforcement

### [VERICIS, Merge Cardio, Model/Catalog Number: Version 12.X, Software Version: 12.0.1, 12.0.2; The VERICIS is an integrated cardiovascular information system classified as a pictu...](https://isitonrecall.com/recall/fda-device-z-1401-2025-vericis-merge-cardio-model-catalog-number-version-12-x-software-version-12-0-1-12-0-2-the-vericis-is/)

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 may be inconsistent with the associated p...

Class II Reported ongoing

Distribution: US

[Official source for VERICIS, Merge Cardio, Model/Catalog Number: Version 12.X, Software Version: 12.0.1, 12.0.2; The ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1401-2025%22)

Feb 19, 2025 FDA device enforcement

### [Merge Cardio, Model/Catalog Number: Version 12.X, Software Version: 12.1, 12.1.1, 12.2, 12.3, 12.3.1, 12.3.2, 12.3.3, 12.4, 12.4.1, 12.4.2; Merge Cardio is a software medical de...](https://isitonrecall.com/recall/fda-device-z-1402-2025-merge-cardio-model-catalog-number-version-12-x-software-version-12-1-12-1-1-12-2-12-3-12-3-1-12-3-2/)

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 may be inconsistent with the associated p...

Class II Reported ongoing

Distribution: US

[Official source for Merge Cardio, Model/Catalog Number: Version 12.X, Software Version: 12.1, 12.1.1, 12.2, 12.3, 12....](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1402-2025%22)

## Reasons in these listed records

- Software issue may cause measurements to be displayed inaccurately.
- Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.
- 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 (Pressure Sensor Defective) during non-invasive blood pressure (N...
- 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 may be inconsistent with the associated primitive measurement...

These examples come from this result page and are not a ranking of every recall reason.

## Checking Merge Healthcare, Inc.

### Is there a recall on merge healthcare, inc. right now?

This archive contains 9 records, including 9 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

[Search Merge Healthcare, Inc.](https://isitonrecall.com/check/?q=Merge%20Healthcare%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
