Device recall
Z-1837-2011: ACUSON S2000 ultrasound systems (all versions) with cardiovascular options…
FDA device recall · Class II · Siemens Medical Solutions USA, Inc., Mountain View, CA
Key facts
| Recall number (Z-number) | Z-1837-2011 |
|---|---|
| Recall event | 56840 |
| Product | ACUSON S2000 ultrasound systems (all versions) with cardiovascular options installed; ACUSON S2000: 10041461; S2000 Cardio Option: 10041853; Product is manufactured and distributed by Siemens Medical Solutions USA, Inc., Business Unit Ultrasound, Mountain View, CA The ACUSON S2000 Ultrasound System… |
| Product code | IYO |
| Recalling firm | Siemens Medical Solutions USA, Inc., Mountain View, CA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 18, 2012 |
| 510(k) numbers | K082142 |
| FEI number | 2936884 |
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