Auto Suture TA 30 Reloadable Staplers, Single Patient Use Ref TA30V3S, V3 (2.5mm) DST Series
FDA device recall Z-0958-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- United States Surgical
- Reason for recall
- Stapler may clamp without the staples being fired into the tissue
- Action taken
- United States Surgical notiied direct accounts by letter dated 5/5/04. Accounts are requested to inventory and quarantine product for return to USS.
- Root cause
- Other
- Status
- Terminated
- Product code
- GDW
- Distribution
- Nationwide
- Date initiated
- 2004-05-05
- Date posted
- 2004-07-20
- Date terminated
- 2006-11-15
- Location
- North Haven, CT
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| AUTO SUTURE SURGICAL STAPLES (K013860) | United States Surgical, A Division of Tyco Healthc | 2001-12-19 |