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U.S. Department of Health and Human Services

Enforcement Report - Week of September 19, 2012

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Product Detail

Product Description Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system
Recall Number Z-2341-2012
Classification Class II
Code Info Model number 5756130 -- serial numbers 6076, 6078, 6080, 6081, and 6082.
Product Distributed Qty 5
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.

Event Detail

Event Id 62988
Product Type Devices
Status Completed
Recalling Firm Siemens Medical Solutions USA, Inc
City Malvern
State PA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-04-30
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide distribution: USA including states of: IN, MI, MS, TN and TX.
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