Device recall
Z-0119-2027: Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241…
FDA device recall · Class II · Intellijoint Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-0119-2027 |
|---|---|
| Recall event | 99821 |
| Product | Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250; Intellijoint HIP, Portable System, REF: 000-0249 |
| Product code | OLO |
| Recalling firm | Intellijoint Surgical, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K191507 |
| FEI number | 3010822102 |
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