Device recall
Z-0546-05: Sodium Chloride Injection USP, manufactured by IV Flush LLC
FDA device recall · Class I · IV Flush LLC
Key facts
| Recall number (Z-number) | Z-0546-05 |
|---|---|
| Recall event | 31082 |
| Product | Sodium Chloride Injection USP, manufactured by IV Flush LLC |
| Product code | FOZ |
| Recalling firm | IV Flush LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 17, 2008 |
| FEI number | 3004978897 |
At a glance
- None Linked 510(k)s
- 1–9 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