Device recall
Z-0444-2007: Puritan Bennett KnightStar 330 Bi-Level Ventilator, Catalogue Numbers…
FDA device recall · Class II · Puritan Bennett Corporation
Key facts
| Recall number (Z-number) | Z-0444-2007 |
|---|---|
| Recall event | 36306 |
| Product | Puritan Bennett KnightStar 330 Bi-Level Ventilator, Catalogue Numbers: Y-KS330-NA, Y-KS330-SD, DSY-KS330-NA, DSY-K5330-SD, DLY-KS330-NA & DLY-KS330-SD |
| Product code | MNT |
| Recalling firm | Puritan Bennett Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 5, 2014 |
| 510(k) numbers | K003075 |
| FEI number | 2024500 |
At a glance
- 1–9 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