Siemens Uroskop Access. Fluoroscopic recall
Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system
Why was Siemens Uroskop Access. Fluoroscopic 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model number 5756130 -- serial numbers 6076, 6078, 6080, 6081, and 6082.
- Product
- Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 5
- Distribution
- Nationwide distribution: USA including states of: IN, MI, MS, TN and TX.
- Recall date
- September 19, 2012
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)