Device recall
Z-0044-2007: 0.9% Sodium Chloride Flush Syringe, 2.5 mL. Product Code: E0100-30. Manufactured…
FDA device recall · Class II · Excelsior Medical Corp
Key facts
| Recall number (Z-number) | Z-0044-2007 |
|---|---|
| Recall event | 35960 |
| Product | 0.9% Sodium Chloride Flush Syringe, 2.5 mL. Product Code: E0100-30. Manufactured by Excelsior Medical and distributed by Hospira, Lake Forest, IL under Hospira''s label, Syrex. |
| Product code | NGT |
| Recalling firm | Excelsior Medical Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 26, 2006 |
| FEI number | 1000122362 |
At a glance
- None 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