Z-0635-05

Mikro-Tip Disposable Angiographic Catheter manufactured by Millar Instruments, Houston, Texas

Name: Z-0635-05 Mikro-Tip Disposable Angiographic Catheter manufactured by Millar Instruments, Houston, Texas
Creator: Millar Instruments, Inc
Published: 2005-01-14
License: https://open.fda.gov/license/

Millar LLC. / initiated 2005-01-14 / Terminated

FDA source

Millar Instruments, Inc began a recall of Mikro-Tip Disposable Angiographic Catheter manufactured by Millar Instruments, Houston, Texas on 2005-01-14. The reason FDA records is "Wire braiding protruding from the catheter". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0635-05
Status: Terminated
Initiated: 2005-01-14
Posted: 2005-03-18
Terminated: 2006-12-19
Recalling firm: Millar LLC.
Product: Mikro-Tip Disposable Angiographic Catheter manufactured by Millar Instruments, Houston, Texas
Product code: DQO Catheter, Intravascular, Diagnostic
Reason for recall: Wire braiding protruding from the catheter.
FDA root cause: Other
Action: The firm initiated the recall via e-mail to direct accounts on 01/14/2005 and letter on 01/20/2005.
Quantity in commerce: 28 catheters
Distribution: Product was distributed to distributors and hospitals in MN, CA, and NY.
Product codes and lots: Lot numbers L034403 and L034731

Product code DQO

K993694Class IIMikro-Tip Angiographic CatheterMillar Instruments, Inc. / cleared 2000-03-01

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)