Z-0730-2007

Flexxus™ Endoscopic Biliary Stent, 7.5 Fr 10 mm diameter x 60 mm length Item Number: LXB10060

Name: Z-0730-2007 Flexxus™ Endoscopic Biliary Stent, 7.5 Fr 10 mm diameter x 60 mm length Item Number: LXB10060
Creator: Conmed Endoscopic Technologies, Inc.
Published: 2007-03-14
License: https://open.fda.gov/license/

Conmed Endoscopic Technologies, Inc. / initiated 2007-03-14 / Terminated

FDA source

Conmed Endoscopic Technologies, Inc. began a recall of Flexxus™ Endoscopic Biliary Stent, 7.5 Fr 10 mm diameter x 60 mm length Item Number: LXB10060 on 2007-03-14. The reason FDA records is "Blue safety clip incorrectly placed on the stent may prevent deployment". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0730-2007
Status: Terminated
Initiated: 2007-03-14
Posted: 2007-04-11
Terminated: 2007-05-15
Recalling firm: Conmed Endoscopic Technologies, Inc.
Product: Flexxus™ Endoscopic Biliary Stent, 7.5 Fr 10 mm diameter x 60 mm length Item Number: LXB10060
Product code: FGE Stents, Drains And Dilators For The Biliary Ducts
Reason for recall: Blue safety clip incorrectly placed on the stent may prevent deployment
FDA root cause: Other
Action: ConMed Endoscopic Technologies notified consignes by letter dated 3/14/07 requesting them to return recalled devices.
Quantity in commerce: 1 UNIT
Distribution: Worldwide distribution, USA including states of DE, OH, MI, DC and countries of Belgium Japan.
Product codes and lots: Lot Number: ANQJ0639

Product code FGE

K031186Class IILuminexx Endoscopic Biliary StentC.R. Bard, Inc. / cleared 2003-05-06

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 2026-09-06. View this recall on fda.gov (opens on fda.gov)