Device recall
Z-0760-2007: Puritan Bennett 840 Ventilator System, Catalogue Numbers: 4-84O12OXXXX-XX…
FDA device recall · Class II · Nellcor Puritan Bennett
Key facts
| Recall number (Z-number) | Z-0760-2007 |
|---|---|
| Recall event | 37607 |
| Product | Puritan Bennett 840 Ventilator System, Catalogue Numbers: 4-84O12OXXXX-XX, 4-840220XXXX-XX, 4-NPB84O-XX, DL4-NPB84O-XX, DS4-NPB840-XX & 4-070550-SP (Note: the Xs indicate any combination of alpha characters which specify option and language packs) |
| Product code | CBK |
| Recalling firm | Nellcor Puritan Bennett |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2012 |
| 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