Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation
Summary
The FDA issued a Class II for Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation by Merge Healthcare, Inc.. Reason: Software issue may cause measurements to be displayed inaccurately..
Details
Source
Device Recall
External ID
Z-3004-2026
Action Date
2026-09-02
Status
Ongoing
Category
device
Product Description
Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation
Lot/Code Info: Software version V9.5 - UDI (01)00842000101239(10)9.5.0(11)260409
Quantity Affected: 20 units
Reason for Recall
Software issue may cause measurements to be displayed inaccurately.
Distribution
US Nationwide distribution in the states of California, Florida, Kentucky, Nebraska, Washington.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-07-22
Company
Hartland, WI
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 168 device recalls issued in the same week, part of 445 device-related FDA actions this month.
Merge Healthcare, Inc. has 9 FDA actions in our database, including 9 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Merge Healthcare, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Merge Healthcare, Inc. have FDA actions?
Merge Healthcare, Inc. has 9 FDA actions in our database, including 9 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-3004-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
Want to know the moment something like this happens?
Get alerts for deviceRelated Actions
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, IC Tray REF: 888810200
Covidien LP · 2023-08-23
Sterile Procedural Trays, labeled as the following: a. BREAST AUGMENTATION b. BREAST REDUCTION CDS c. CUH ABDOMINO
MEDLINE INDUSTRIES, LP - Northfield · 2023-02-15
VTC Regular Kit Nephrostomy Catheter System Kit, Material Number REF M001245300; to provide external drainage of the uri
Boston Scientific Corporation · 2024-09-25
EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx; Summit Indoo
Enchroma Inc · 2024-11-27
Otological Ventilation Tube - T-Tube 9mm - Silicone; Product Code: NZ3309;
Adept Medical Ltd · 2025-01-29