Device recall
Z-0559-06: Acclarent brand Relieva Sinus Inflation Device Kit; Model BID30; The kit…
FDA device recall · Class II · Acclarent Inc
Key facts
| Recall number (Z-number) | Z-0559-06 |
|---|---|
| Recall event | 34524 |
| Product | Acclarent brand Relieva Sinus Inflation Device Kit; Model BID30; The kit contains 1 inflation device, 1-10'' extension tube, 1-20cc syringe, 3-way stop-cock; Manufactured for Acclarent, Inc., 1525-B O''Brien Dr., Menlo Park, CA 94025 |
| Product code | LRC |
| Recalling firm | Acclarent Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 11, 2006 |
| 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