Device recall
Z-1318-2024: Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set…
FDA device recall · Class II · Think Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-1318-2024 |
|---|---|
| Recall event | 94086 |
| Product | Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System |
| Product code | OLO |
| Recalling firm | Think Surgical, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K230202 |
| FEI number | 3000719653 |
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