Angiodynamics, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0712-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

MICRO-PSD HDR, Catalog Number: PSD-HB5N - 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.

Product Classification:

Class II

Date Initiated: November 19, 2019

Date Posted: December 25, 2019

Recall Number: Z-0712-2020

Event ID: 84382

Reason for Recall:

May result in readings outside of the expected accuracy range.

Status: Terminated

Product Quantity: 60 units

Code Information:

Lot Numbers: 118881, 118929, 119750 UDI:00851546007714

Distribution Pattern:

US Nationwide distribution in the states of AZ, GA, MA, NJ, NY, OH, PA.

Voluntary or Mandated:

Voluntary: Firm initiated