Device recall
Z-2268-2011: Case Label: REORDER NO. 7203 (STERILE) CSR WRAP WELCON BRAND FOLEY CATHETER TRAY…
FDA device recall · Class II · Nurse Assist, Inc
Key facts
| Recall number (Z-number) | Z-2268-2011 |
|---|---|
| Recall event | 58021 |
| Product | Case Label: REORDER NO. 7203 (STERILE) CSR WRAP WELCON BRAND FOLEY CATHETER TRAY w/o Catheter w/10ml. Prefilled Syringe 20 ea/Box 800-649-6800 3400 Northern Cross Blvd. Fort Worth, TX 76137 www.nurseassist.com MADE IN U.S.A. Tray Label: REORDER NO. 7203 STERILE UNLESS OPENED OR DAMAGED nurse assist… |
| 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