Device recall
Z-0926-2017: Normal Saline Flush 0.9% USP Sodium Chloride Injection Syringe, 3 ml fill, 5 ml…
FDA device recall · Class I · Nurse Assist, Inc
Key facts
| Recall number (Z-number) | Z-0926-2017 |
|---|---|
| Recall event | 75348 |
| Product | Normal Saline Flush 0.9% USP Sodium Chloride Injection Syringe, 3 ml fill, 5 ml fill and 10 ml fill. Product codes: 1203, 1205, 1210, 1210-BP Product usage: Saline flush |
| Product code | NGT |
| Recalling firm | Nurse Assist, Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 16, 2017 |
| 510(k) numbers | K150143 |
| FEI number | 3002695476 |
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