Device recall
Z-2071-2015: Exactech Single Barrel Drill Guides The Single Barrel Drill Guide is a…
FDA device recall · Class II · Exactech, Inc.
Key facts
| Recall number (Z-number) | Z-2071-2015 |
|---|---|
| Recall event | 71501 |
| Product | Exactech Single Barrel Drill Guides The Single Barrel Drill Guide is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. |
| Product code | KWQ |
| Recalling firm | Exactech, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 16, 2015 |
| 510(k) numbers | K143576 |
| FEI number | 1038671 |
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