PlainRecalls
FDA Devices Moderate Class II Terminated

Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system

Reported: September 19, 2012 Initiated: April 30, 2012 #Z-2341-2012

Product Description

Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system

Reason for Recall

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.

Details

Units Affected
5
Distribution
Nationwide distribution: USA including states of: IN, MI, MS, TN and TX.
Location
Malvern, PA

Frequently Asked Questions

What product was recalled?
Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 5.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 19, 2012. Severity: Moderate. Recall number: Z-2341-2012.