Xcision Medical Systems recalls GammaPod Treatment Planning System due to risk of selecting incorrect CT scans for radiation treatment. Affected units have specific model numbers and distribution dates.
Wrong structures imported into the GammaPod Treatment Planning System.-system allowed an RTSS generated from a previous CT scan to be selected
Xcision Medical Systems is recalling its GammaPod Treatment Planning System component because it can incorrectly select CT scans from previous treatments. This could lead to improper radiation dosing during breast cancer treatment. Affected users should contact the manufacturer for details.
The system allows radiation treatment planning software to select CT scans from previous treatments incorrectly. This could result in improper radiation dosing during breast cancer treatment, potentially affecting treatment effectiveness.
Medical professionals using the GammaPod system for breast radiation treatment. Patients receiving breast cancer treatment with this system are most at risk.
Check for model numbers: TPS0018, TPS0013, TPS0016, or TPS0014. Units distributed in the US between specific dates as listed in the recall notice.
Identify your GammaPod Treatment Planning System model number from the list provided in the recall notice.
The system can incorrectly select CT scans from previous treatments, which may lead to improper radiation dosing during breast cancer treatment.
Check for model numbers TPS0018, TPS0013, TPS0016, or TPS0014 as listed in the recall notice.
Contact Xcision Medical Systems directly for further instructions on the recall.
We’ve drafted a message you can send Xcision Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0750-2024 — Xcision Medical Systems Xcision Medical Systems Hello, I own a Xcision Medical Systems that is covered by recall Z-0750-2024 from Xcision Medical Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
