Device recall
Z-0108-2008: Olympus Single Use Mechanical Lithotriptor, Model number BML-201Q, Olympus…
FDA device recall · Class III · Olympus America Inc.
Key facts
| Recall number (Z-number) | Z-0108-2008 |
|---|---|
| Recall event | 44929 |
| Product | Olympus Single Use Mechanical Lithotriptor, Model number BML-201Q, Olympus America, Inc. |
| Product code | LQC |
| Recalling firm | Olympus America Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 15, 2008 |
| 510(k) numbers | K903529 |
| FEI number | 2429304 |
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