Elekta, Inc.: Medical Device Recall in 2013 - (Recall #: Z-2276-2013)

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:

Monaco RTP System Radiation treatment planning

Product Classification:

Class II

Date Initiated: July 2, 2013

Date Posted: October 2, 2013

Recall Number: Z-2276-2013

Event ID: 65996

Reason for Recall:

Upgrade installation script is designed to overwrite the same pouch files in the Treatment Couch Library with the original default values.

Status: Terminated

Product Quantity: 45

Code Information:

Versions 3.10.00 and later

Distribution Pattern:

Nationwide Distribution including AK, CA, CO, CT, FL, IL, IN, MI, MN, MO, NC, NJ, NY, OH, OK, OR, PA, SC, TN, TX, WA and Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated