Device recall
Z-0081-04: Sonotrode Probe, a straight nephroscopy probe with a 3.5 mm diameter and 362 mm…
FDA device recall · Class II · Richard Wolf Medical Instrument Corp
Key facts
| Recall number (Z-number) | Z-0081-04 |
|---|---|
| Recall event | 27489 |
| Product | Sonotrode Probe, a straight nephroscopy probe with a 3.5 mm diameter and 362 mm working length; an accessory to the Richard Wolf Model 2271 Ultrasound Generator Unit 2271; Richard Wolf Medical Instruments Corp., Vernon Hills, IL 60061 |
| Product code | FFK-- |
| Recalling firm | Richard Wolf Medical Instrument Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 10, 2004 |
| 510(k) numbers | K011065 |
| FEI number | 1418479 |
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