Device recall
Z-0031-2026: Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF…
FDA device recall · Class I · Percussionaire Corporation
Key facts
| Recall number (Z-number) | Z-0031-2026 |
|---|---|
| Recall event | 97374 |
| Product | Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use |
| Product code | BZO |
| Recalling firm | Percussionaire Corporation |
| Recall class | Class I |
| 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