Micrus brand WATUSI Guidewire 0.014'' - Soft Tip, Catalog Number; WST 140205-00; Distributed by Micrus Endovascular Corp
FDA device recall Z-1542-06 · posted 2006-09-29 · Terminated
Recall details
- Recalling firm
- Micrus Endovascular Corporation
- Reason for recall
- During use, the introducer may cause the guide wire''s coating to strip off and may result in loose material which could break free and enter the blood stream.
- Action taken
- On 9/8/06 the firm issued letters via Federal Express to all its direct consignees, informing them of the affected product and providing instructions on the recall.
- Root cause
- Other
- Status
- Terminated
- Product code
- DQX
- Quantity affected
- 413 units
- Distribution
- Worldwide
- Date initiated
- 2006-09-08
- Date posted
- 2006-09-29
- Date terminated
- 2007-06-29
- Location
- San Jose, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| MICRUS GUIDE WIRE, WATUSI 0.014 (K053265) | Micrus Endovascular Corporation | 2006-04-28 |