Medtronic MiniMed Model 7311Version 5.0A Solutions Pumps and Meters Software
FDA device recall Z-0265-04 · posted 2003-12-24 · Terminated
Recall details
- Recalling firm
- Medtronic MiniMed
- Reason for recall
- Accessory software fails to report certain reports following download of data from 712 pump.
- Action taken
- 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
- Status
- Terminated
- Product code
- LZG
- Quantity affected
- 1020
- Distribution
- Nationwide, Canada, Europe, Middle East and Africa
- Date initiated
- 2003-11-19
- Date posted
- 2003-12-24
- Date terminated
- 2005-03-03
- Location
- Northridge, CA
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