Device recall
Z-1808-2015: T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10…
FDA device recall · Class II · MRP, LLC dba AMUSA
Key facts
| Recall number (Z-number) | Z-1808-2015 |
|---|---|
| Recall event | 70974 |
| Product | T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL Single Use Syringe, Rx only, Part no. 2S0706 Usage: Flush syringe. |
| Product code | NGT |
| Recalling firm | MRP, LLC dba AMUSA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 22, 2015 |
| 510(k) numbers | K120836 |
| 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