General Electric Med Systems Seneographe 700T Mammography X-Ray Systems Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Seneographe 700T Mammography X-Ray Systems
Brand
General Electric Med Systems
Lot Codes / Batch Numbers
All serial numbers
Products Sold
All serial numbers
General Electric Med Systems is recalling Seneographe 700T Mammography X-Ray Systems due to The mammography system's information for users lacked the technical specification for the minimum filtration permanently installed in the useful beam . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The mammography system's information for users lacked the technical specification for the minimum filtration permanently installed in the useful beam and the technical specification for the maximum line current.
Recommended Action
Per FDA guidance
The consignees were sent 'Regulatory Notice' letters dated February 6, 2004. The letters informed the consignees of the violations and provided them with the technical specifications which needed to be provided.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026