Z-0169-04

Ambulatory infusion pump. Model 511

Name: Z-0169-04 Ambulatory infusion pump. Model 511
Creator: Medtronic MiniMed
Published: 2003-09-09
License: https://open.fda.gov/license/

Medtronic, Inc. / initiated 2003-09-09 / Terminated

FDA source

Medtronic MiniMed began a recall of Ambulatory infusion pump. Model 511 on 2003-09-09. The reason FDA records is "Non delivery of insulin by pump after electrostatic discharge". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0169-04
Status: Terminated
Initiated: 2003-09-09
Posted: 2003-11-27
Terminated: 2005-09-02
Recalling firm: Medtronic, Inc.
Product: Ambulatory infusion pump. Model 511
Product code: LZG Pump, Infusion, Insulin
Reason for recall: Non delivery of insulin by pump after electrostatic discharge.
FDA root cause: Other
Quantity in commerce: 17,000
Distribution: Nationwide Canada and possibly International
Product codes and lots: No information at this time.

Product code LZG

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)