Atlas FDA

SenoScan True View Digital Mammography System

FDA device recall Z-0939-04 · posted 2004-07-20 · Terminated

Recall details

Recalling firm
Fischer Imaging Corporation
Reason for recall
X-ray tube may overheat after high usage because of mis-wired thermal switch circuit.
Action taken
Customers were notified by certified mail on 4/19/2004.
Root cause
Other
Status
Terminated
Product code
ITY
Quantity affected
37
Distribution
Nationwide CA, CO, FL, IN, MA, MO, NC, NY, OK, TX, WI, Mexico, France. No government or military distribution.
Date initiated
2004-04-12
Date posted
2004-07-20
Date terminated
2004-07-26
Location
Denver, CO

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