Device recall
Z-1730-2015: Low Volume Extension Set, 72' w/Clamp FLL/MLL APV=1.3ml, STERILE, AND FLUID PATH…
FDA device recall · Class II · Smiths Medical Asd Inc
Key facts
| Recall number (Z-number) | Z-1730-2015 |
|---|---|
| Recall event | 71142 |
| Product | Low Volume Extension Set, 72' w/Clamp FLL/MLL APV=1.3ml, STERILE, AND FLUID PATH NONPYROGENIC UNLESS PACKAGE IS DAMAGED OR OPENED. LATEX FREE, SINGLE USE Tyvek pouches, 10 per box, Smiths Medical ASD, Inc. Used to administer fluid and drugs intravenously. |
| Product code | FPA |
| Recalling firm | Smiths Medical Asd Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 20, 2016 |
| 510(k) numbers | K831087 |
| FEI number | 1526863 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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