Ambulatory infusion pump. Model 511
FDA device recall Z-0169-04 · posted 2003-11-27 · Terminated
Recall details
- Recalling firm
- Medtronic MiniMed
- Reason for recall
- Non delivery of insulin by pump after electrostatic discharge.
- Root cause
- Other
- Status
- Terminated
- Product code
- LZG
- Quantity affected
- 17,000
- Distribution
- Nationwide Canada and possibly International
- Date initiated
- 2003-09-09
- Date posted
- 2003-11-27
- Date terminated
- 2005-09-02
- Location
- Northridge, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.