Device recall
Z-1549-2008: Medex MX821L 72 inch (182.9cm) Administration Sets, Standard Drip, Sterile…
FDA device recall · Class III · Smiths Medical Asd Inc
Key facts
| Recall number (Z-number) | Z-1549-2008 |
|---|---|
| Recall event | 47474 |
| Product | Medex MX821L 72 inch (182.9cm) Administration Sets, Standard Drip, Sterile Single Use, Latex Free device packaged 25 units per case. Used to administer fluids. |
| Product code | LHI |
| Recalling firm | Smiths Medical Asd Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 30, 2010 |
| 510(k) numbers | K790314 |
| FEI number | 1526863 |
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