Health product recall

TrueBeam, TrueBeam STx, and TrueBeam Edge (2018-08-22)

Starting date:
August 22, 2018
Posting date:
September 7, 2018
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-67694

Affected products

  1. TrueBeam
  2. TrueBeam STx
  3. TrueBeam Edge

Reason

Unintended override of gated treatment plan.

Affected products

A. TrueBeam

Lot or serial number
  • Serial #: H191075
  • Serial #: H191332
  • Serial #: H191333
  • Serial #: H191417
  • Serial #: H191491
  • Serial #: H191650
  • Serial #: H191652
  • Serial #: H191676
  • Serial #: H192169
  • Serial #: H192703
Model or catalog number
  • Versions 2.0
  • Versions 2.5
Companies
Manufacturer

Varian Medical Systems, Inc.

3100 Hansen Way

Palo Alto

94304

California

UNITED STATES


B. TrueBeam STx

Lot or serial number
  • Serial #:  H191038
  • Serial #: H191318
  • Serial #: H191321
Model or catalog number
  • Versions 2.0
  • Versions 2.5
Companies
Manufacturer

Varian Medical Systems, Inc.

3100 Hansen Way

Palo Alto

94304

California

UNITED STATES


C. TrueBeam Edge

Lot or serial number

Serial #: H192301

Model or catalog number
  • Versions 2.0
  • Versions 2.5
Companies
Manufacturer

Varian Medical Systems, Inc.

3100 Hansen Way

Palo Alto

94304

California

UNITED STATES