GE Inspection Technologies, LP: Medical Device Recall in 2015 - (Recall #: Z-2320-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

GE Optional Laser Centering Device X-ray generator.

Product Classification:

Class II

Date Initiated: November 10, 2014

Date Posted: August 19, 2015

Recall Number: Z-2320-2015

Event ID: 69849

Reason for Recall:

GE has identified a potential failure to comply with 21 C.F.R. ¿ 1040.10 and 21 C.F.R. ¿ 1010.2 for the alignment laser centering device.

Status: Terminated

Product Quantity: 25

Code Information:

Model No. 025.03.00A

Distribution Pattern:

US Distribution to the states of : NY, CA, WA, PA, MD, AL, FL and LA.

Voluntary or Mandated:

Voluntary: Firm initiated