Device recall
Z-0407-06: SonoSite L25 Needle Guide Kit, 21 GAUGE, Part Number P04053-01. Manufactured…
FDA device recall · Class III · Sonosite, Inc.
Key facts
| Recall number (Z-number) | Z-0407-06 |
|---|---|
| Recall event | 34250 |
| Product | SonoSite L25 Needle Guide Kit, 21 GAUGE, Part Number P04053-01. Manufactured for: SonoSite, Inc., Bothell, WA 98021 Each kit is packaged in a hermetically sealed clear plastic pouch with white backing. Product is labeled as Sterile. 24 pouches are packaged in a white cardboard box and labeled as… |
| Product code | ITX |
| Recalling firm | Sonosite, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 31, 2006 |
| 510(k) numbers | K030064 |
| FEI number | 3002087856 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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