Health product recall

Pinnacle³ Radiation Therapy Planning System

Last updated

Summary

Product
Pinnacle³ Radiation Therapy Planning System
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalog number
Pinnacle³ 16.2.1 Not applicable. 459801419352
Pinnacle³ 16.2.1 Not applicable. 459801421292

Issue

There is a software issue affecting Pinnacle³ Radiation Therapy Planning System performing advanced region of interest (ROI) expansion and contraction that results in a potential shift of the intended ROI. The software assumes the patient is always in the head first supine (HFS) position when transposing the advanced expansion to alternate positions.

While performing advanced region of interest (ROI) expansion and contraction in the HFS position, the tool works as intended. However, when performing advanced ROI expansion and contraction on HFP, FFS, or FFP orientation images sets, a direction error occurs which results in potential overdose to nearby structure or potential underdose in the treatment plan.

The following steps will lead to the software issue described above:

  1. Therapist / physician performs simulation based on HFP, FFS, and FFP images
  2. Physician performs advanced variable ROI expansion/contraction
  3. There is an error in direction of expansion/contraction

Recall start date: June 11, 2025

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies

Philips Medical Systems (Cleveland), Inc.

3630 Sw 47th Avenue, Gainesville, Florida, United States, 32608

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-77629

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