Device recall
Z-0864-03: Acuson Diagnostic Ultrasound System Transducer; Model Number(s): L582 Linear…
FDA device recall · Class III · Siemens Medical Solutions USA, Inc.
Key facts
| Recall number (Z-number) | Z-0864-03 |
|---|---|
| Recall event | 26006 |
| Product | Acuson Diagnostic Ultrasound System Transducer; Model Number(s): L582 Linear Array Transducer for use on the 128XP Ultrasound System; Catalog Numbers: 23656 (New), 45441 (Refurb) |
| Product code | MAA |
| Recalling firm | Siemens Medical Solutions USA, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 22, 2003 |
| 510(k) numbers | K884632 |
| FEI number | 2936884 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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