Device recall
Z-0637-2024: High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only…
FDA device recall · Class I · Percussionaire Corporation
Key facts
| Recall number (Z-number) | Z-0637-2024 |
|---|---|
| Recall event | 93476 |
| Product | High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123 |
| Product code | CBK |
| Recalling firm | Percussionaire Corporation |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K905234 |
| FEI number | 1000524541 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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