GE Medical Systems, SCS: Medical Device Recall in 2024 - (Recall #: Z-1780-2024)

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:

GE Healthcare Allia IGS 7, Interventional fluoroscopic x-ray systems

Product Classification:

Class II

Date Initiated: March 18, 2024

Date Posted: May 15, 2024

Recall Number: Z-1780-2024

Event ID: 94305

Reason for Recall:

GE HealthCare has become aware of the potential that adhesive material might not have been applied to some bolts of certain Innova IGS, Discovery IGS, Interact IGS, Allia IGS and Allia Pulse IGS products. This could result in a potential fall of the Detector/Elevator or X-ray tube of the frontal Gantry assembly.

Status: Ongoing

Product Quantity: 6 units

Code Information:

UDI/DI 00195278215543, Serial Numbers: D4-23-035, D4-23-036, D4-23-038, D4-23-042, D4-24-001, D4-24-003

Distribution Pattern:

Worldwide distribution - US Nationwide in the states of CA, FL, GA, IN, MA, NC, OK, SC, TN, TX, VA and the countries of Armenia, China, France, Hungary, India, Italy, Japan, Kazakhstan, Lithuania, Mexico, Russia, Spain, Taiwan, Turkey, Vietnam

Voluntary or Mandated:

Voluntary: Firm initiated