Device recall
Z-1800-2012: Vygon VY(TM)Flush Heparin Lock Flush Syringes, 100 Units per mL, 3mL in a 10mL…
FDA device recall · Class II · Vygon Corporation
Key facts
| Recall number (Z-number) | Z-1800-2012 |
|---|---|
| Recall event | 61945 |
| Product | Vygon VY(TM)Flush Heparin Lock Flush Syringes, 100 Units per mL, 3mL in a 10mL Flush Syringe, 30 syringes per box, Rx only Prefilled syringes are used to maintain the patency of indwelling catheter lumens |
| Product code | NZW |
| Recalling firm | Vygon Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 11, 2013 |
| 510(k) numbers | K061497 |
| FEI number | 2245270 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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