Device recall
Z-0458-2023: Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF…
FDA device recall · Class II · Intersect ENT, Inc.
Key facts
| Recall number (Z-number) | Z-0458-2023 |
|---|---|
| Recall event | 91063 |
| Product | Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044 |
| Product code | OWO |
| Recalling firm | Intersect ENT, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3008301917 |
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