Device recall
Z-1113-2017: Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone…
FDA device recall · Class II · Flower Orthopedics Corporation
Key facts
| Recall number (Z-number) | Z-1113-2017 |
|---|---|
| Recall event | 76156 |
| Product | Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set. |
| Product code | LXH |
| Recalling firm | Flower Orthopedics Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 27, 2017 |
| FEI number | 3009996260 |
At a glance
- None 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