Device recall
Z-0052-2020: K2M Special Connector Instruments (Special Connector, Special Adaptor, and Quick…
FDA device recall · Class II · K2M, Inc
Key facts
| Recall number (Z-number) | Z-0052-2020 |
|---|---|
| Recall event | 83777 |
| Product | K2M Special Connector Instruments (Special Connector, Special Adaptor, and Quick Adaptor) Product Usage: Special Connector Instruments include an additional feature on their shafts that enable surgeon users to combine them with non-K2M navigation systems as part of their standard surgical technique. |
| Product code | OLO |
| Recalling firm | K2M, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 22, 2020 |
| 510(k) numbers | K171321 |
| FEI number | 3008599177 |
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