FDAFDA · Food and drugs·Recall number Z-2341-2012
Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system
Published September 19, 2012 · Recall initiated: April 30, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Siemens Medical Solutions USA, Inc
- Distributor
- Nationwide distribution: USA including states of: IN, MI, MS, TN and TX.
- Lot
- Model number 5756130 -- serial numbers 6076, 6078, 6080, 6081, and 6082.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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