Z-1477-05

Vaxcel Chest Ports - Mini/T/S/8/1.5/2.6/63 Catalog Number : 45-310

Name: Z-1477-05 Vaxcel Chest Ports - Mini/T/S/8/1.5/2.6/63 Catalog Number : 45-310
Creator: Boston Scientific Corporation
Published: 2005-07-22
License: https://open.fda.gov/license/

Boston Scientific Corporation / initiated 2005-07-22 / Terminated

FDA source

Boston Scientific Corporation began a recall of Vaxcel Chest Ports - Mini/T/S/8/1.5/2.6/63 Catalog Number : 45-310 on 2005-07-22. The reason FDA records is "The Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1477-05
Status: Terminated
Initiated: 2005-07-22
Posted: 2005-09-02
Terminated: 2007-06-20
Recalling firm: Boston Scientific Corporation
Product: Vaxcel Chest Ports - Mini/T/S/8/1.5/2.6/63 Catalog Number : 45-310
Product code: KOB Catheter, Suprapubic (And Accessories)
Reason for recall: The Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use.
FDA root cause: Other
Action: Boston Scientific intiated the recall on 7/22/05 to direct accounts and to distributors on 7/ 27 /05. Distributors are requested to conduct sub recalls to the medical facility level. A revised letter dated 8/2/05 was sent to 18 US accounts for one lot (#1020895) omitted in the letter of 7/22/05.
Distribution: Nationwide VA Hopsitals Foreign: Canada, Africa, Japan, Israel, Japan, Nertherlands, Venezula
Product codes and lots: Lot Numbers: 897963 899779 905283 905540 905795 912253 912714 918871 919149 920316 926376 926666 934740 935754 937478 938097 938491 942049 942282 948073 953631 958509 958815 959675 968284 968734 969544 970794 972100 974707 975769 976229 978021 980595 981357 991171 991172 991173 991174 991438 992989 1000900 1000901 1000902 1001276 1002352

Product code KOB

K030083Class IIVaxcel with Pasv PortBoston Scientific Corp / cleared 2003-01-28

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)