Varian Medical Systems Imaging Laboratory GmbH: Medical Device Recall in 2022 - (Recall #: Z-0942-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

ARIA Radiation Therapy Management (RTM) VERSIONS 13.6, 15.1, 15.5, 15.6, 16.0, 16.1

Product Classification:

Class II

Date Initiated: March 21, 2022

Date Posted: April 20, 2022

Recall Number: Z-0942-2022

Event ID: 89922

Reason for Recall:

Software issue for treatment plan and image management application may result in mismatch values which could result in treatment in the wrong location

Status: Completed

Product Quantity: 14

Code Information:

DI Numbers: 00856100006066, 00856100006080, 00856100006097, 00856100006110, 00856100006127,00856100006165

Distribution Pattern:

Worldwide distribution - US Nationwide distribution in the states of MI, KS, OH, VA, DC, FL, PA, OK, MN, AZ and the countries of South Korea, Netherlands, Poland, China.

Voluntary or Mandated:

Voluntary: Firm initiated