Angiodynamics recalls PSD-PE5N radiation sensors used in cancer treatment that may give inaccurate radiation readings. Affected units have specific lot numbers and UDI codes. Consumers should contact the company for details.
May result in readings outside of the expected accuracy range.
Angiodynamics is recalling pre-calibrated radiation sensors used in cancer treatment that may give inaccurate radiation readings. This could affect treatment planning and patient safety if not corrected.
These sensors measure radiation therapy doses during cancer treatment. If they give inaccurate readings, treatment planning could be compromised, potentially affecting patient safety.
Patients receiving cancer radiation therapy using these sensors may be affected. Medical professionals using the sensors for treatment planning are most at risk.
Check for lot numbers 106020, 106:030, or 119400 on the sensor. The unique device identifier (UDI) 00851546007141 is also associated with these units.
Reach out to Angiodynamics for specific instructions on how to verify if your sensor is affected.
The recall states they may give inaccurate readings, so they are not recommended for use until corrected.
Check for lot numbers 106020, 106030, or 119400 and UDI 00851546007141 on the sensor.
Contact Angiodynamics for specific instructions on how to verify and address the issue.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-0713-2020 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-0713-2020 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.
