Mikro-Tip Disposable Angiographic Catheter manufactured by Millar Instruments, Houston, Texas
FDA device recall Z-0635-05 · posted 2005-03-18 · Terminated
Recall details
- Recalling firm
- Millar Instruments, Inc
- Reason for recall
- Wire braiding protruding from the catheter.
- Action taken
- The firm initiated the recall via e-mail to direct accounts on 01/14/2005 and letter on 01/20/2005.
- Root cause
- Other
- Status
- Terminated
- Product code
- DQO
- Quantity affected
- 28 catheters
- Distribution
- Product was distributed to distributors and hospitals in MN, CA, and NY.
- Date initiated
- 2005-01-14
- Date posted
- 2005-03-18
- Date terminated
- 2006-12-19
- Location
- Houston, TX
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| MIKRO-TIP ANGIOGRAPHIC CATHETER (K993694) | Millar Instruments, Inc. | 2000-03-01 |