Device recall
Z-1740-2015: RELIEVA FLEX Sinus Guide Catheter F-70. Catalog number GC070RF. Product Usage…
FDA device recall · Class III · Acclarent, Inc.
Key facts
| Recall number (Z-number) | Z-1740-2015 |
|---|---|
| Recall event | 71232 |
| Product | RELIEVA FLEX Sinus Guide Catheter F-70. Catalog number GC070RF. Product Usage - Sinus Catheter - Intended to provide a means to access the sinus space for diagnostic and therapeutic procedures. . |
| Product code | KAM |
| Recalling firm | Acclarent, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 10, 2015 |
| FEI number | 3005172759 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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