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

Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system — recall Z-2341-2012

U.S. FDA — Device Enforcement · United States · 2012-04-30 · Class II

As described by U.S. FDA — Device Enforcement: Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2341-2012
Date of alert
2012-04-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Medical Solutions USA, Inc
Product category
device
Product type
Devices
Recall status
Terminated — the recall action is complete and the FDA has closed it
Initiated by
Voluntary: Firm initiated
Distribution
Nationwide distribution: USA including states of: IN, MI, MS, TN and TX.
Reported risk: Siemens has discovered a possible hazard to patients or hospital personnel when tilting the Uroskop Access system starting with serial number 6076. When tilting the table on the Uroskop Access table, the motor may become disconnected and the entire table assembly may fall on the floor.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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