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

Recall Z-0921-2017 — SOMATOM Perspective, Computed tomography x-ray system

U.S. FDA — Device Enforcement · United States · 2016-11-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0921-2017
Date of alert
2016-11-22
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Medical Solutions USA, Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10967888
Reported risk: Siemens is providing a new installation of the Residual Current Monitor (RCM) in the Line Connection Box (LCB) to resolve a potential defect that could lead to a power cutout during use of the SOMATOM Scope, Scope Power and Perspective systems.
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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