Device recall
Z-0926-04: ACMI REF E-3F Electrohydraulic Lithotripsy Probe, 3 FR x 120CM
FDA device recall · Class II · ACMI CORPORATION
Key facts
| Recall number (Z-number) | Z-0926-04 |
|---|---|
| Recall event | 28975 |
| Product | ACMI REF E-3F Electrohydraulic Lithotripsy Probe, 3 FR x 120CM |
| Product code | FFK |
| Recalling firm | ACMI CORPORATION |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 13, 2005 |
| 510(k) numbers | K980492 |
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