Z-1219-04

Cook brand Zenith rupture main body graft, preloaded graft measuring 26 mm diameter at promial end and 12 mm...

Name: Z-1219-04 Cook brand Zenith rupture main body graft, preloaded graft measuring 26 mm diameter at promial end and 12 mm...
Creator: Cook, Inc.
Published: 2004-06-10
License: https://open.fda.gov/license/

Cook Incorporated / initiated 2004-06-10 / Terminated

FDA source

Cook, Inc. began a recall of Cook brand Zenith rupture main body graft, preloaded graft measuring 26 mm diameter at promial end and 12 mm diameter at distal end, with the H&L-B One Shot... on 2004-06-10. The reason FDA records is "Introducer tubing may contain a vein of unextruded material and carbon black or a strand of tubing material may be displaced from the introducer during use". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1219-04
Status: Terminated
Initiated: 2004-06-10
Posted: 2004-07-27
Terminated: 2004-11-01
Recalling firm: Cook Incorporated
Product: Cook brand Zenith rupture main body graft, preloaded graft measuring 26 mm diameter at promial end and 12 mm diameter at distal end, with the H&L-B One Shot Introducer System, non-sterile, export only for further processing; ZRB-26-WCE.
Product code: MIH System, Endovascular Graft, Aortic Aneurysm Treatment
Reason for recall: Introducer tubing may contain a vein of unextruded material and carbon black or a strand of tubing material may be displaced from the introducer during use.
FDA root cause: Other
Action: The firm issued recall letters to customers on 6/10/04. The recall was extended and URGENT EXTENSION OF PRODUCT RECALL notices were sent out on June 23, 2004.
Quantity in commerce: 19
Distribution: Nationwide, Canada, Denmark and Japan.
Product codes and lots: Lots F1544276, F1544277, F1544279, F1544280, F1544278, F1554515, F1554516, F1554517, F1554518, F1554519, F1554520, F1554521, F1554523, F1554524, F1554525, F1554522, F1554526, F1554527 and F1554528.

Product code MIH

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)