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Terminated

MediSpectra Luma Cervical Imaging System Model Number: 3-02600

FDA Recall Z-0988-2007 · Posted 2007-07-03

Recalling FirmMedispectra Inc.
Recall StatusTerminated
Product CodeMWM
Date Initiated2007-05-15
Date Terminated2007-07-09
Product Quantity8 units

Reason for Recall

Power supply may fail and render the unit inoperable.

Firm Action

MediSpectra notified users by telephone on 5/15/07 and follow-up letter. Users are requested to select a date for field servce to replace the power supply.

Root Cause

Other

Distribution Pattern

AZ, CA, FL, & NY.

Official Source

View FDA Recall →

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

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