Z-0739-03

Boston Scientific/Microvasive Cone Tip Ureteral Catheter (7 Fr x 70 cm) Product Number: 400-213

Name: Z-0739-03 Boston Scientific/Microvasive Cone Tip Ureteral Catheter (7 Fr x 70 cm) Product Number: 400-213
Creator: Boston Scientific Corporation
Published: 2003-03-17
License: https://open.fda.gov/license/

Boston Scientific Corporation / initiated 2003-03-17 / Terminated

FDA source

Boston Scientific Corporation began a recall of Boston Scientific/Microvasive Cone Tip Ureteral Catheter (7 Fr x 70 cm) Product Number: 400-213 on 2003-03-17. The reason FDA records is "Warning flag may be detached from the tip protector on the catheter and result in the tip protector advancing through the catheter during use". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0739-03
Status: Terminated
Initiated: 2003-03-17
Posted: 2003-04-17
Terminated: 2016-03-07
Recalling firm: Boston Scientific Corporation
Product: Boston Scientific/Microvasive Cone Tip Ureteral Catheter (7 Fr x 70 cm) Product Number: 400-213
Product code: GBM Catheter, Urethral
Reason for recall: Warning flag may be detached from the tip protector on the catheter and result in the tip protector advancing through the catheter during use
FDA root cause: Other
Action: Boston Scientific/Microvasive, Natick, MA notified domestic accounts by letter on 3/17/03. Users are requesed to check inventory and return product to Boston Scientific. A responsed form was requested to be completed. and returned by facsmile.
Quantity in commerce: 6 boxes (20 units/box)
Distribution: Nationwide Foreign:Singapore, Japan, Korea, Canada, Africa
Product codes and lots: Lot Numbers: 5218586 5218586 5303655 5312172 5348155

Product code GBM

K870694Class IIVan-Tec Open Ended Cone Tip Ureteral CatheterVan-Tec, Inc. / cleared 1987-03-10

Hollister recalls 2.5 million intermittent catheters over a manufacturing defect11 SEP 2026 / by Medical Device Manufacturing

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)