PTW NORTH AMERICA CORPORATION: Medical Device Recall in 2022 - (Recall #: Z-0479-2022)

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:

Software BeamAdjust version 2.2, Catalog No: S070009 Software VeriSoft version 8.0, Catalog No: S080032

Product Classification:

Class II

Date Initiated: August 27, 2021

Date Posted: January 19, 2022

Recall Number: Z-0479-2022

Event ID: 89314

Reason for Recall:

When a measurement with a PTW detector array is performed with the software BeamAdjust 2.2 or VeriSoft 8.0, a measurement error can occur under specific conditions. This error can lead to a too-low or too-high measured absolute dose which affects patient plan verification results

Status: Terminated

Product Quantity: 1 unit

Code Information:

S/N :AU2001094-1 UDI: EPTWS0700090 VeriSoft ;EPTWS0700090 BeamAdjust

Distribution Pattern:

US Nationwide distribution in the state of CO.

Voluntary or Mandated:

Voluntary: Firm initiated