GE Healthcare GmbH: Medical Device Recall in 2024 - (Recall #: Z-3145-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

ViewPoint; system, imaging processing, radiological

Product Classification:

Class II

Date Initiated: August 8, 2024

Date Posted: September 25, 2024

Recall Number: Z-3145-2024

Event ID: 95167

Reason for Recall:

The National Institute of Standards and Technology (NIST) has identified in the National Vulnerability Database (NVD) that NexGen Healthcare Mirth Connect, prior to version 4.4.1, has a potential vulnerability allowing the deserialization of untrusted data (CVE-2023-43208). Mirth products may have been installed and configured with your ViewPoint / ViewPoint 6 system by GE HealthCare. This vulnerability could allow a malicious actor to access the system and potentially manipulate patient data.

Status: Ongoing

Product Quantity: 3 units

Code Information:

No UDI/DI, System ID numbers: QB7A TA99, N26D M0B7, Q1K1 FFQW

Distribution Pattern:

US Nationwide distribution including in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin.

Voluntary or Mandated:

Voluntary: Firm initiated