Device recall
Z-0551-2011: Dixtal Handheld Pulse Oximetry Model 512 Catalog Number: 9100-00
FDA device recall · Class II · Dixtal Medical, Inc.
Key facts
| Recall number (Z-number) | Z-0551-2011 |
|---|---|
| Recall event | 57045 |
| Product | Dixtal Handheld Pulse Oximetry Model 512 Catalog Number: 9100-00 |
| Product code | DQA |
| Recalling firm | Dixtal Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 4, 2016 |
| 510(k) numbers | K032949 |
| FEI number | 3006891479 |
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