Device recall
Z-0035-2011: Excelsior Disposable Syringe W/Normal Saline (0.9% sodium Chloride) General…
FDA device recall · Class I · Excelsior Medical Corp
Key facts
| Recall number (Z-number) | Z-0035-2011 |
|---|---|
| Recall event | 56685 |
| Product | Excelsior Disposable Syringe W/Normal Saline (0.9% sodium Chloride) General hospital use |
| Product code | NGT |
| Recalling firm | Excelsior Medical Corp |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 23, 2012 |
| 510(k) numbers | K090882 |
| 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