FDA Medical Device Recalls (openFDA)
Medtronic MiniMed: Medtronic MiniMed Model 7311Version 5.0A Solutions Pumps and Meters Software
- Recall number
- Z-0265-04
- Recalling firm
- Medtronic MiniMed
- Product
- Medtronic MiniMed Model 7311Version 5.0A Solutions Pumps and Meters Software
- Status
- Terminated
- Initiated
- 2003-11-19
- Posted
- 2003-12-24
- Terminated
- 2005-03-03
- Reason
- Accessory software fails to report certain reports following download of data from 712 pump.
- Root cause
- Other
- Action
- Sales personnel will visit each center and install the software and leave a CD. Or, instructions will be FEDEXed with a CD.
- Quantity
- 1020
- Distribution
- Nationwide, Canada, Europe, Middle East and Africa
- Lot, serial or model codes
- version 5.0A
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LZG
- Firm FEI
- 3003166194
- Firm city
- Northridge
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28