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Terminated

Medtronic MiniMed Model 7311Version 5.0A Solutions Pumps and Meters Software

FDA Recall Z-0265-04 · Posted 2003-12-24

Recalling FirmMedtronic MiniMed
Recall StatusTerminated
Product CodeLZG
Date Initiated2003-11-19
Date Terminated2005-03-03
Product Quantity1020

Reason for Recall

Accessory software fails to report certain reports following download of data from 712 pump.

Firm Action

Sales personnel will visit each center and install the software and leave a CD. Or, instructions will be FEDEXed with a CD.

Root Cause

Other

Distribution Pattern

Nationwide, Canada, Europe, Middle East and Africa

Official Source

View FDA Recall →

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

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