Device recall
Z-2075-2015: Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical…
FDA device recall · Class II · Musculoskeletal Transplant Foundation, Inc.
Key facts
| Recall number (Z-number) | Z-2075-2015 |
|---|---|
| Recall event | 71559 |
| Product | Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific needs of the orthopedic surgeon and are intended to be used in conjunction with the associated allograft. This kit is for single use only. |
| Product code | HXY |
| Recalling firm | Musculoskeletal Transplant Foundation, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2017 |
| FEI number | 3001236616 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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