Device recall
Z-0319-2009: AS3000 Anesthesia Delivery System. Datascope Patient Monitoring; A Mindray…
FDA device recall · Class II · Mindray DS USA, Inc., dba Datascope Patient Monitoring
Key facts
| Recall number (Z-number) | Z-0319-2009 |
|---|---|
| Recall event | 49713 |
| Product | AS3000 Anesthesia Delivery System. Datascope Patient Monitoring; A Mindray Global Company. The AS3000 is a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. |
| Product code | BSZ |
| Recalling firm | Mindray DS USA, Inc., dba Datascope Patient Monitoring |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 8, 2008 |
| 510(k) numbers | K080175 |
| FEI number | 2221819 |
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