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

Recall Z-2403-2019 — SOMATOM go.All; Models #11061638 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data

U.S. FDA — Device Enforcement · United States · 2019-07-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2403-2019
Date of alert
2019-07-31
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)
11061638
Reported risk: The injector holder could potentially fall off together with the injector and the storage box.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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