Elekta, Inc.: Medical Device Recall in 2012 - (Recall #: Z-2340-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Multileaf Collimator To be used for single or multiple fractions, delivered as static and/or dynamic beams of radiation, in all areas of the body where such treatment is indicated.

Product Classification:

Class II

Date Initiated: July 27, 2012

Date Posted: September 19, 2012

Recall Number: Z-2340-2012

Event ID: 62915

Reason for Recall:

Information released with the product Agility did not originally contain information on compatibility with the add-on Dynamic Multileaf Collimator Apex.

Status: Terminated

Product Quantity: 2

Code Information:

152599 and 152678

Distribution Pattern:

Nationwide Distribution including DC & MD

Voluntary or Mandated:

Voluntary: Firm initiated