Recall Z-0523-2012

Siemens Medical Solutions USA, Inc · initiated September 15, 2011

Terminated

Product

MAMMOMAT Inspiration Full field digital mammographic x-ray system

Codes / lots: Model number 10140000

Reason for recall

Lowering the swivel arm with "object table" while an operator's or patient's body parts are underneath the "object table" may cause the "object table" to collide with and injure the operator or patient. Therefore attention should be paid when adjusting "object table" height to avoid a possible risk of injury to the operator or the patient. The movement of the swivel arm may also cause an injur

FDA-determined cause: Use error

Action taken

Siemens Medical Solutions USA, Inc sent a Safety Advisory Notice dated January 8, 2011, to all affected customers. The letter identified the product, the problem and the action needed to be taken by the customer. The notification included an Addendum to the User Manual. We appreciate your understanding and cooperation with this safety advisory and ask you to immediately instruct your operating personnel accordingly. Please ensure that this safety advisory is placed in the System's Operator Manual. Your operating personnel should maintain awareness over an appropriate defined period. Further questions please call (610) 219-4834.

Details

Recall number
Z-0523-2012
Initiated
September 15, 2011
Posted by FDA
January 11, 2012
Terminated
March 5, 2014
Product code
MUE – Full Field Digital, System, X-Ray, Mammographic
Quantity
12
Distribution
Nationwide Distribution including the states of FL, MD, MI, NE, NY, NC, ND, OH, and SC.
Recalling firm
Siemens Medical Solutions USA, Inc, Malvern, PA

Official FDA recall record