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Angiodynamics, Inc. recalls MICRO-PSD EXTERNAL BEAM PHOTON, Catalog Number: PSD-PE5N - Product Usage: pre-calibrated PSD sensors are intended for us
Recalled December 25, 2019 · FDA recall Z-0713-2020 · Angiodynamics
Hazard
May result in readings outside of the expected accuracy range. · FDA Class II
Units
48 units
Sold at
US Nationwide distribution in the states of AZ, GA, MA, NJ, NY, OH, PA.
Description
May result in readings outside of the expected accuracy range.
Product
MICRO-PSD EXTERNAL BEAM PHOTON, Catalog Number: PSD-PE5N - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to measure photon and electron radiation therapy as an adjunct to treatment planning permitting measurement and validation of radiation dose received by the patient to the targeted area of their body.
Manufacturer(s)
Angiodynamics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →