Angiodynamics recalls MICRO-PSD HDR cancer radiation sensors (lot 118881, 118929, 119750) that may give inaccurate radiation measurements during cancer treatment.
May result in readings outside of the expected accuracy range.
Angiodynamics is recalling cancer radiation sensors that may give inaccurate readings during treatment. This could lead to improper radiation dose measurements, potentially affecting treatment safety.
These sensors are designed to measure radiation therapy doses during cancer treatment. If they give inaccurate readings, the radiation dose delivered to the patient's targeted area might be incorrect.
Patients undergoing cancer radiation therapy who use these sensors for dose measurement. Those with specific lot numbers are most at risk.
Check for lot numbers 118881, 118929, or 119750 on the product label. The product is a pre-calibrated sensor used in cancer radiation therapy.
Look for lot numbers 118881, 118929, or 119750 on the sensor label.
The sensors may give readings outside the expected accuracy range during cancer radiation treatment.
Check the lot number on the product label. If it matches 118881, 118929, or 119750, contact Angiodynamics for guidance.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-0712-2020 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-0712-2020 from Angiodynamics. 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.
