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

Recall Z-1036-2017 — Olympus Scientific Solutions Americas Corporation (OSSA) VANTA¿ XRF Analyzer. Model Vanta VCR and Vanta VMR Analytical X-ray systems

U.S. FDA — Device Enforcement · United States · 2017-01-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1036-2017
Date of alert
2017-01-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Olympus Scientific Solutions Americas
Product category
device
Product type
Devices
Reported risk: It was discovered under rare circumstances the LED warning light circuit could fail. If this happens, while the instrument is emitting X-rays during at test, the LED warning lights will not illuminate. The test runs normally and will execute as before, but the light will not be on.
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.

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