Device recall
Z-1939-2009: The BladderScan BVI 9400 is a portable ultrasound instrument that provides a…
FDA device recall · Class II · Verathon, Inc.
Key facts
| Recall number (Z-number) | Z-1939-2009 |
|---|---|
| Recall event | 52769 |
| Product | The BladderScan BVI 9400 is a portable ultrasound instrument that provides a noninvasive measurement of urinary bladder volume. The device consists of an ultrasound probe that scans the patient's bladder, and a battery operated console that provides measurement related information. The BVI 9400… |
| Product code | IYO |
| Recalling firm | Verathon, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 7, 2010 |
| 510(k) numbers | K071217 |
| 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