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

Recall Z-0300-2019 — Ysio MAX (model number 10762470) with Tube stand 3D V (model number 7042018 or 7042034), radiographic systems used in radiographic and tomographic exposures of the whole body.

U.S. FDA — Device Enforcement · United States · 2018-08-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0300-2019
Date of alert
2018-08-06
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)
10762470
Reported risk: In rare cases of high clinical workload, the steel cables inside the lifting column of the overhead tube, which are designed to take the load, may rapture without triggering the safety lock. This could lead to overloading the safety rope, which is not designed for continuous load and ongoing movement under load. This may lead to mechanical fatigue and cause the arm to drop down unexpectedly during movement in vertical direction and during patient positioning.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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