Device recall
Z-0672-2008: Parks Medical Ultrasonic Doppler Flow Detector, Model 811-BTS (finished assembly…
FDA device recall · Class III · Parks Medical Electronics Inc
Key facts
| Recall number (Z-number) | Z-0672-2008 |
|---|---|
| Recall event | 45800 |
| Product | Parks Medical Ultrasonic Doppler Flow Detector, Model 811-BTS (finished assembly without accompanying probes), Parks Medical Electronics, Inc., Aloha, OR 97007 |
| Product code | DPW |
| Recalling firm | Parks Medical Electronics Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 13, 2011 |
| FEI number | 3020115 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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