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Terminated

SenoScan Full Field Digital Mammography System--Product Number 94001G-3, 105200G

FDA Recall Z-0757-06 · Posted 2006-04-11

Recalling FirmFischer Imaging Corporation
Recall StatusTerminated
Product CodeMUE
Date Initiated2006-03-27
Date Terminated2012-03-13
Product Quantity80 units.(Domestic) Foreign list pending

Reason for Recall

Software upgrade to preclude lost images during mammography procedure.

Firm Action

Consignees were notified by letter on 03/27/2006.

Root Cause

Other

Distribution Pattern

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.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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