Lorad, A Division of Hologic Lorad M-IV Mammography System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Lorad M-IV Mammography System
Brand
Lorad, A Division of Hologic
Lot Codes / Batch Numbers
S/N''s :18005960001 to 18010034196
Products Sold
S/N''s :18005960001 to 18010034196
Lorad, A Division of Hologic is recalling Lorad M-IV Mammography System due to System failed to meet the mA's accuracy specfications at low mA's values. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
System failed to meet the mA's accuracy specfications at low mA's values
Recommended Action
Per FDA guidance
Lorad notified customers/dealers by letter dated January 14, 2004. Sites were advised of the corrected Accuracy labeling.
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