GE Inspection Technologies, LP: Medical Device Recall in 2016 - (Recall #: Z-1231-2016)

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 Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.

Product Classification:

Class II

Date Initiated: December 16, 2015

Date Posted: April 13, 2016

Recall Number: Z-1231-2016

Event ID: 73364

Reason for Recall:

GE Inspection Technologies, LP ("GE") has discovered that certain of its cabinet x-ray systems may not fully comply with the Food and Drug Administration's (FDA) Cabinet X¿ ray System performance standards, 21 C.F.R. ¿ 1020.40(c)(1)(i)

Status: Terminated

Product Quantity: 55 US Distribution

Code Information:

phoenix micrornelx and nanomelx cabinet x-ray systems

Distribution Pattern:

US Distribution to the states of : TX, MD, MI, CA, TN, NH, NY, AL, NC, ID, MA, AZ, IN, FL, PA, NJ, WI, VA, MN, MD CO, GA, SC, OH and DC.

Voluntary or Mandated:

Voluntary: Firm initiated