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

Recall Z-1652-2014 — Siemens Linear Accelerator (LINAC) models. Product Usage: deliver X-ray radiation for therapeutic treatment of cancer

U.S. FDA — Device Enforcement · United States · 2014-04-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1652-2014
Date of alert
2014-04-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Medical Solutions USA, Inc
Product category
device
Product type
Devices
Reported risk: Siemens Radiation Oncology became aware that customers may be using the Siemens Linear Accelerator in combination with stereotactic accessories which have not been validated as being compatible with Siemens LINAC models.
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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