Device recall
Z-3319-2026: Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065; Phasitron…
FDA device recall · Class II · Percussionaire Corporation
Key facts
| Recall number (Z-number) | Z-3319-2026 |
|---|---|
| Recall event | 99617 |
| Product | Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065; Phasitron 5 Breathing Circuit with Unified Connector, Product Number: P5-UC, used with In-Line Valve Instruction Manual |
| Product code | NHJ |
| Recalling firm | Percussionaire Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1000524541 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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