Device recall
Z-1220-04: Battery Pack Respironics Model 915 for use in the 900 Series SmartMonitor and…
FDA device recall · Class II · Respironics, Inc.
Key facts
| Recall number (Z-number) | Z-1220-04 |
|---|---|
| Recall event | 29333 |
| Product | Battery Pack Respironics Model 915 for use in the 900 Series SmartMonitor and the 900 Series Pulse Oximeter. |
| Product code | BZQ |
| Recalling firm | Respironics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 6, 2005 |
| FEI number | 2518422 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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