FDA Recall Terminated

GE SENOGRAPHE ESSENTIAL FULL FIELD MAMMOGRAPHY SYSTEM ( SENO ESSENTIAL) The expected usage of this product is for the same clinical applications as traditional mammographic film/screen systems. It generates mammographic images which can be used for screening and diagnosis of breast cancer.

Recall: Z-1043-2011 · Initiated July 20, 2010

Recall

Recall Number
Z-1043-2011
Event Number
57763
Firm
GE Healthcare, LLC
FEI Number
2126677
Product Code
MUE
Status
Terminated
Root Cause
Radiation Control for Health and Safety Act
Initiated
July 20, 2010
Posted
March 17, 2011
Terminated
May 16, 2012
Address
3000 N Grandview Blvd, Waukesha, WI, 53188-1615

Description

GE SENOGRAPHE ESSENTIAL FULL FIELD MAMMOGRAPHY SYSTEM ( SENO ESSENTIAL) The expected usage of this product is for the same clinical applications as traditional mammographic film/screen systems. It generates mammographic images which can be used for screening and diagnosis of breast cancer.

Reason

It was noticed that 3 units received in Japan were missing the rating plate on the X-ray tube cover. There is a potential that other X-ray tube covers are missing the rating plate.

Action

An Important Electronic Product Radiation Warning letter was issued to customers identifying the affected product and describing the defect along with the related hazards. The letter states that there are no actions that are required to be taken on the part of the customer. A GE Healthcare Service Representative will apply the missing rating as necessary and free of charge. Questions or concerns regarding the letter should be directed to 1-800-437-1171 in the US.

Distribution

Worldwide Distribution

Quantity

112 total