Device recall
Z-2725-2011: IQecg IQdevices SDK, Part Numbers: 4-100-1403, Software Version 8.3.2 Product…
FDA device recall · Class II · Brentwood Medical Technology Corp
Key facts
| Recall number (Z-number) | Z-2725-2011 |
|---|---|
| Recall event | 56016 |
| Product | IQecg IQdevices SDK, Part Numbers: 4-100-1403, Software Version 8.3.2 Product Usage: IQecg is to be used, under the supervision of a Physician, to obtain Electrocardiograms from the human body surface. |
| Product code | DSI |
| Recalling firm | Brentwood Medical Technology Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 22, 2011 |
| 510(k) numbers | K955023 |
| FEI number | 2081230 |
At a glance
- 1–9 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