Ambulatory infusion pump. Model 511
FDA Recall Z-0169-04 · Posted 2003-11-27
Recalling FirmMedtronic MiniMed
Recall StatusTerminated
Product CodeLZG
Date Initiated2003-09-09
Date Terminated2005-09-02
Product Quantity17,000
Reason for Recall
Non delivery of insulin by pump after electrostatic discharge.
Root Cause
Other
Distribution Pattern
Nationwide Canada and possibly International
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.