Device recall
Z-2193-2013: *** 1) Cat. 4341B; Qty. 10; Thoracentesis Tray; With Catheter; Sterile…
FDA device recall · Class II · Carefusion 2200 Inc
Key facts
| Recall number (Z-number) | Z-2193-2013 |
|---|---|
| Recall event | 66123 |
| Product | *** 1) Cat. 4341B; Qty. 10; Thoracentesis Tray; With Catheter; Sterile; CareFusion; 1500 Waukegan Road; McGaw Park, IL 60085 USA; *** 2) Cat. 4341BSDF; Qty. 10; Safe-T Thoracentesis Tray; With Catheter and Sharps Injury Protection; Drug Free; CareFusion; 1500 Waukegan Road; McGaw Park, IL 60085 USA… |
| Product code | GCB |
| Recalling firm | Carefusion 2200 Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 16, 2015 |
| FEI number | 3008002452 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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