Pinnacle 3 with TumorLOC, (870258) Radiation Therapy Planning System Software — FDA record Z-2239-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 17, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Pinnacle 3 with TumorLOC, (870258) Radiation Therapy Planning System Software
Reason
Due to software issue, Radiation Therapy Planning system may provide incorrect dataset calculations when performing the "Stopping Power Ratio" (SPR) ,
Classification
Class II
Recalling firm
Philips Medical Systems (Cleveland) Inc
Quantity
149 Serial Numbers
Agency-reported status
Ongoing
Source record identifier
Z-2239-2025

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilitySoftware Version Number: 18.0.5/UDI: (01)00884838103566

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Worldwide - US Nationwide distribution in the state of WV and the countries of Macao & United Kingdom.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Aug 13, 2025
Recall initiation date
Jul 17, 2025
Center classification date
Aug 1, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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