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U.S. Department of Health and Human Services

Enforcement Report - Week of June 20, 2012

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Product Detail

Product Description GE Proteus XR/a Radiographic System. GE Medical Systems-Americas Milwaukee, WI. Model Number: 2259988. Product is indicated for use in generating radiographic images of human anatomy in all general-purpose diagnostic procedures. This device is not intended for mammographic applications.
Recall Number Z-1790-2012
Classification Class II
Code Info All serial numbers
Product Distributed Qty 3,796 units
Reason For Recall An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Proteus XR/a Table while moving the tabletop with the thumb placed over its edge and fingers underneath

Event Detail

Event Id 37654
Product Type Devices
Status Completed
Recalling Firm General Electric Med Systems LLC
City Waukesha
State WI
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2006-05-31
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Worldwide Distribution.
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