SenoScan Full Field Digital Mammography System--Product Number 94001G-3, 105200G
FDA device recall Z-0757-06 · posted 2006-04-11 · Terminated
Recall details
- Recalling firm
- Fischer Imaging Corporation
- Reason for recall
- Software upgrade to preclude lost images during mammography procedure.
- Action taken
- Consignees were notified by letter on 03/27/2006.
- Root cause
- Other
- Status
- Terminated
- Product code
- MUE
- Quantity affected
- 80 units.(Domestic) Foreign list pending
- Distribution
- Nationwide. AZ, CA, CO, FL, GA, IL, IN, KS, MA, MI, MN, MT, NY, OK, SC, TX, WA, WI, WV. No government or military consignees.
- Date initiated
- 2006-03-27
- Date posted
- 2006-04-11
- Date terminated
- 2012-03-13
- Location
- Denver, CO
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