Z-0794-2007

Boston Scientific Medi-Tech Stainless Steel Greenfield Vena Cava Filter, order #50-400, lot #7826572

Name: Z-0794-2007 Boston Scientific Medi-Tech Stainless Steel Greenfield Vena Cava Filter, order #50-400, lot #7826572
Creator: Boston Scientific
Published: 2006-10-06
License: https://open.fda.gov/license/

Boston Scientific Corporation / initiated 2006-10-06 / Terminated

FDA source

Boston Scientific began a recall of Boston Scientific Medi-Tech Stainless Steel Greenfield Vena Cava Filter, order #50-400, lot #7826572 on 2006-10-06. The reason FDA records is "One lot of product, Stainless Steel Greenfield Vena Cava Filter, may have the incorrect expiration date of 2008-07 and the correct date is 2008-06". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0794-2007
Status: Terminated
Initiated: 2006-10-06
Posted: 2007-05-10
Terminated: 2012-07-03
Recalling firm: Boston Scientific Corporation
Product: Boston Scientific Medi-Tech Stainless Steel Greenfield Vena Cava Filter, order #50-400, lot #7826572
Product code: DTK Filter, Intravascular, Cardiovascular
Reason for recall: One lot of product, Stainless Steel Greenfield Vena Cava Filter, may have the incorrect expiration date of 2008-07 and the correct date is 2008-06.
FDA root cause: Other
Action: Consignees were notified by letter (10/06/2006) which was accompanied by a Reply Verification Letter. All consignees were asked to cease use of product upon receipt of the letter and to fax the Reply Verification Letter to recalling firm and return product to firm.
Quantity in commerce: 24 units
Distribution: Nationwide.
Product codes and lots: Lot #7826572

Product code DTK

K964284Class IIStainless Steel Greenfield Vena Cava Filter with 12F Introducer SystemBoston Scientific Corp / cleared 1997-01-06

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 2026-09-05. View this recall on fda.gov (opens on fda.gov)