Device recall
Z-1007-2024: ExcelsiusGPS Cannula A, 9mm x 250mm, Cannula used with ball tip probes, Model…
FDA device recall · Class II · Globus Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1007-2024 |
|---|---|
| Recall event | 93804 |
| Product | ExcelsiusGPS Cannula A, 9mm x 250mm, Cannula used with ball tip probes, Model No. 6143.2844 |
| Product code | OLO |
| Recalling firm | Globus Medical, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K171651 |
| FEI number | 3004142400 |
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