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Terminated

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

FDA Recall Z-0635-05 · Posted 2005-03-18

Recalling FirmMillar Instruments, Inc
Recall StatusTerminated
Product CodeDQO
Date Initiated2005-01-14
Date Terminated2006-12-19
Product Quantity28 catheters

Reason for Recall

Wire braiding protruding from the catheter.

Firm Action

The firm initiated the recall via e-mail to direct accounts on 01/14/2005 and letter on 01/20/2005.

Root Cause

Other

Distribution Pattern

Product was distributed to distributors and hospitals in MN, CA, and NY.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K993694MIKRO-TIP ANGIOGRAPHIC CATHETERMillar Instruments, Inc. · 2000-03-01

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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