FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system
- Recall number
- Z-2341-2012
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system
- Status
- Terminated
- Initiated
- 2012-04-30
- Posted
- 2012-09-10
- Terminated
- 2012-09-20
- Reason
- 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.
- Root cause
- Nonconforming Material/Component
- Action
- Siemens sent a Update instructions letter dated April 2012, to all affected customers. The safety instruction letter identified the product the problem and the action needed to be taken by the customer. The update has been completed successfully. The customer has been informed of the benefits of improvements resulting from this update. Further questions please call (610) 219-4834.
- Quantity
- 5
- Distribution
- Nationwide distribution: USA including states of: IN, MI, MS, TN and TX.
- Lot, serial or model codes
- Model number 5756130 -- serial numbers 6076, 6078, 6080, 6081, and 6082.
- 510(k) numbers
- ["K010942"]
- PMA numbers
- not on file
- Product code
- JAA
- Firm FEI
- 2240869
- Firm city
- Malvern
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
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Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28