Elekta, Inc.: Medical Device Recall in 2013 - (Recall #: Z-0885-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Elekta, Apex add-on Micro MLC, collimator for radiation therapy.

Product Classification:

Class II

Date Initiated: January 18, 2013

Date Posted: March 6, 2013

Recall Number: Z-0885-2013

Event ID: 64213

Reason for Recall:

If the Apex collimator is incorrectly installed on the radiation head, a touchguard inhibit activates the view restrictions dialog box only shows the top 12 restrictions.

Status: Terminated

Product Quantity: 1

Code Information:

152652

Distribution Pattern:

Nationwide Distribution including TX

Voluntary or Mandated:

Voluntary: Firm initiated