Regulatory Insight, Inc: Medical Device Recall in 2016 - (Recall #: Z-0753-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

GE Precision MPi is an all-digital multipurpose tilt-C x-ray system, intended for a multitude of diagnostic procedures, including radiology, fluoroscopy, interventional procedures, vascular and non-vascular procedures, and specialized applications including angiographic studies.

Product Classification:

Class II

Date Initiated: July 1, 2008

Date Posted: March 2, 2016

Recall Number: Z-0753-2016

Event ID: 72515

Reason for Recall:

It was discovered that the Remote Touch Panel (RTP) of the GE Precision MPi X-ray system may not always boot up as intended and needs to be updated to properly accomplish its intended purpose.

Status: Terminated

Product Quantity: 43

Code Information:

NRT no.: 02980000

Distribution Pattern:

US Distribution to the states of :TN, CA, WA, OR, PA, WI, FL, MN, VT, NY, NV, MA, CO, IN, MI, MS and OH.

Voluntary or Mandated:

Voluntary: Firm initiated