Device recall
Z-0003-2011: BVI 9600 Bladder Volume Instrument, Aorta Scan Mode The BladderScan BVI 9600…
FDA device recall · Class II · Verathon, Inc.
Key facts
| Recall number (Z-number) | Z-0003-2011 |
|---|---|
| Recall event | 56411 |
| Product | BVI 9600 Bladder Volume Instrument, Aorta Scan Mode The BladderScan BVI 9600 with AortaScan Mode is a user-selectable, dual-function ultrasound device that projects ultrasound energy either into the lower abdomen to obtain an image of the bladder for measuring bladder volume, or into the mid-abdomen… |
| Product code | IYO |
| Recalling firm | Verathon, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 8, 2011 |
| 510(k) numbers | K082456 |
| FEI number | 3022472 |
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