Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0710-2020 — OARtrac PLUS CLINICAL DETECTOR UNIT Catalog Number: OTS-V2-Plus - 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 rece

U.S. FDA — Device Enforcement · United States · 2019-11-19 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0710-2020
Date of alert: 2019-11-19
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Angiodynamics, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00851546007196

Reported risk: May result in readings outside of the expected accuracy range.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Related