Fischer Imaging Corporation SenoScan Full Field Digital Mammography System--Product Number 94001G-3, 105200G Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SenoScan Full Field Digital Mammography System--Product Number 94001G-3, 105200G
Brand
Fischer Imaging Corporation
Lot Codes / Batch Numbers
Software versions earlier than 5.2.2 Product Number 94001G-3, 105200G
Products Sold
Software versions earlier than 5.2.2 Product Number 94001G-3, 105200G
Fischer Imaging Corporation is recalling SenoScan Full Field Digital Mammography System--Product Number 94001G-3, 105200G due to Software upgrade to preclude lost images during mammography procedure.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software upgrade to preclude lost images during mammography procedure.
Recommended Action
Per FDA guidance
Consignees were notified by letter on 03/27/2006.
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