Device recall
Z-1692-2008: Puritan-Bennett 800 Series Ventilator Backup Power Source (BPS) Model 802…
FDA device recall · Class II · Covidien Limited
Key facts
| Recall number (Z-number) | Z-1692-2008 |
|---|---|
| Recall event | 47523 |
| Product | Puritan-Bennett 800 Series Ventilator Backup Power Source (BPS) Model 802, Puritan-Bennett Corporation, A subsidiary of Mallinckrodt Inc., Carlsbad, CA |
| Product code | CBK |
| Recalling firm | Covidien Limited |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2008 |
| 510(k) numbers | K970460 |
| FEI number | 2936999 |
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