RAYSEARCH LABORATORIES AB: Medical Device Recall in 2020 - (Recall #: Z-1467-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

RayStation/RayPlan 9A, Build Number 9.0.0.113, stand-alone software treatment planning system

Product Classification:

Class II

Date Initiated: February 20, 2020

Date Posted: March 18, 2020

Recall Number: Z-1467-2020

Event ID: 85065

Reason for Recall:

There is a potential for erroneous propagation of the current tabletop positions when applying pitch or roll correction. Even though pitch and roll correction is never propagated, non-zero pitch or roll causes the lateral, longitudinal and vertical values propagated to be incorrect.

Status: Terminated

Product Quantity: 1 system in the U.S.

Code Information:

UDI 07350002010174

Distribution Pattern:

The products were distributed to the following US states: TN

Voluntary or Mandated:

Voluntary: Firm initiated