Device recall
Z-0973-2009: Sterile Field Saline Flush; 0.9% Sodium Chloride Injection, USP; Rx Only; Single…
FDA device recall · Class II · Excelsior Medical Corp
Key facts
| Recall number (Z-number) | Z-0973-2009 |
|---|---|
| Recall event | 50848 |
| Product | Sterile Field Saline Flush; 0.9% Sodium Chloride Injection, USP; Rx Only; Single Use. Excelsior Medical, Neptune, NJ. This product is used for the flushing of venous access devices and intravenous tubing. |
| Product code | NGT |
| Recalling firm | Excelsior Medical Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 6, 2009 |
| 510(k) numbers | K053120 |
| FEI number | 1000122362 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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