Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

SenoScan True View Digital Mammography System

FDA Recall Z-0939-04 · Posted 2004-07-20

Recalling FirmFischer Imaging Corporation
Recall StatusTerminated
Product CodeITY
Date Initiated2004-04-12
Date Terminated2004-07-26
Product Quantity37

Reason for Recall

X-ray tube may overheat after high usage because of mis-wired thermal switch circuit.

Firm Action

Customers were notified by certified mail on 4/19/2004.

Root Cause

Other

Distribution Pattern

Nationwide CA, CO, FL, IN, MA, MO, NC, NY, OK, TX, WI, Mexico, France. No government or military distribution.

Official Source

View FDA Recall →

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

↑