Device recall
Z-1221-06: TriActiv System Balloon Inflation Syringe. The syringe packs/boxes contain 5…
FDA device recall · Class II · Kensey Nash Corp
Key facts
| Recall number (Z-number) | Z-1221-06 |
|---|---|
| Recall event | 35680 |
| Product | TriActiv System Balloon Inflation Syringe. The syringe packs/boxes contain 5 'spare' syringes. |
| Product code | NFA |
| Recalling firm | Kensey Nash Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 11, 2006 |
| 510(k) numbers | K042040 |
| FEI number | 1000307073 |
At a glance
- 1–9 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