Device recall
Z-1709-2015: 0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx…
FDA device recall · Class II · MRP, LLC dba AMUSA
Key facts
| Recall number (Z-number) | Z-1709-2015 |
|---|---|
| Recall event | 71175 |
| Product | 0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe. |
| Product code | NGT |
| Recalling firm | MRP, LLC dba AMUSA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 2, 2016 |
| 510(k) numbers | K133685 |
| FEI number | 1000151124 |
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