Device recall
Z-2267-2011: Case Label: REORDER NO. 7202 (STERILE) CSR WRAP WELCON BRAND URETHRAL CATHETER…
FDA device recall · Class II · Nurse Assist, Inc
Key facts
| Recall number (Z-number) | Z-2267-2011 |
|---|---|
| Recall event | 58021 |
| Product | Case Label: REORDER NO. 7202 (STERILE) CSR WRAP WELCON BRAND URETHRAL CATHETER TRAY with 14 french red rubber catheter Caution: Contains Natural Latex nurse assist incorporated 20 ea/Box 800-649-6800 3400 Northern Cross Blvd. Fort Worth, TX 76137 www.nurseassist.com Tray Label: REORDER NO. 7202… |
| Product code | KOD |
| Recalling firm | Nurse Assist, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 25, 2012 |
| FEI number | 3002695476 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database