Z-0979-06

CATH. GUIDE 7F SR4.0 W/SH LAUN CATHETER LA7SR40SH LA 7F 100CM SR40 Coronary Guiding catheter designed to...

Name: Z-0979-06 CATH. GUIDE 7F SR4.0 W/SH LAUN CATHETER LA7SR40SH LA 7F 100CM SR40 Coronary Guiding catheter designed to...
Creator: Medtronic, Inc.
Published: 2006-04-05
License: https://open.fda.gov/license/

Medtronic, Inc. / initiated 2006-04-05 / Terminated / root cause: packaging

FDA source

Medtronic, Inc. began a recall of CATH. GUIDE 7F SR4.0 W/SH LAUN CATHETER LA7SR40SH LA 7F 100CM SR40 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or... on 2006-04-05. The reason FDA records is "Potential for non-sterility due to loss of package integrity". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-0979-06
Status: Terminated
Initiated: 2006-04-05
Posted: 2006-06-01
Terminated: 2007-06-20
Recalling firm: Medtronic, Inc.
Product: CATH. GUIDE 7F SR4.0 W/SH LAUN CATHETER LA7SR40SH LA 7F 100CM SR40 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peripheral vascular system. Product Code: LA7SR40SH
Product code: DQY Catheter, Percutaneous
Reason for recall: Potential for non-sterility due to loss of package integrity
Root cause tag: packaging
FDA root cause: Other
Action: Medtronic notified accounts and sales representatives on 4/05/06 advising the recalled product be segregated and held for return to the sales rep. and documented on the reconciliation form.
Quantity in commerce: 110 units
Distribution: Nationwide Foreign: Austria, Australia, Bahrain, Bulgaria, Canada, Czech Republic, Denmark, Germany, Hungary, Italy, Jordan, France, Greece, Japan, Hong Kong, India, Italy, Norway, Poland, Portugal, Saudi Arabia, Spain, Sweden, Switzerland, UK.
Product codes and lots: Lot Numbers: 0000005212 0000043605 0000053798 0000056337 0000068436 0000068560 0000071683 0000076651 0000108452 0000137727 0000164243 176812 208561 212698 213441 217363

Product code DQY

K022764Class II7F Launcher Guide CatheterMedtronic Vascular / cleared 2002-08-28

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)