Angiodynamics recalls OARtrac PLUS Clinical Detector Units (catalog OTS-V2-Plus) with specific lot numbers due to potential inaccuracies in radiation therapy measurements. Affected units may not provide correct radiation dose readings during cancer treatment.
May result in readings outside of the expected accuracy range.
Angiodynamics is recalling OARtrac PLUS Clinical Detector Units (catalog number OTS-V2-Plus) with specific lot numbers because they may give inaccurate radiation dose readings during cancer treatment. This could affect treatment planning and patient safety.
The pre-calibrated PSD sensors in the device may not measure radiation doses accurately during cancer treatment. This could lead to incorrect treatment planning if the device is used to validate radiation dose received by the patient.
Cancer patients receiving radiation therapy who use this detector unit for treatment planning. Healthcare providers using the device for radiation dose validation are most at risk.
Check for the catalog number OTS-V2-Plus on the unit. Affected units have specific lot numbers: 025-001-055-A-003, 025-001-055-A-005, 025-001-055-A-007, and 025-001-055-A-008.
Look for the lot numbers 025-001-055-A-003, 025-001-055-A-005, 025-001-055-A-007, or 025-001-055-A-008 on the device.
The device may give inaccurate radiation dose readings during cancer treatment, which could affect treatment planning.
Check the lot number on the device. If it matches the affected numbers, contact Angiodynamics for guidance.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-0710-2020 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-0710-2020 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.
