Device recall
Z-0740-2012: U-Joint Hex Head Driver 3.5mm, Part Number 228-0016, for the Escalade Acetabular…
FDA device recall · Class II · Ortho Development Corporation
Key facts
| Recall number (Z-number) | Z-0740-2012 |
|---|---|
| Recall event | 60722 |
| Product | U-Joint Hex Head Driver 3.5mm, Part Number 228-0016, for the Escalade Acetabular Cup System. Driver is included in Part Number 270-9004-Escalade Acetabular Prep Kit and Part Number 228-9001-Triplus Acetabular Instrument Kit. The Acetabular Cup System is indicated for use in total hip arthroplasty… |
| Product code | LZO |
| Recalling firm | Ortho Development Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 27, 2012 |
| 510(k) numbers | K103384 |
| FEI number | 3017298928 |
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