Device recall
Z-0113-2022: Flower Drill Bit Kit 2.7mm- The Drill Bit Kit, 2.7mm (DBK 027) is intended to be…
FDA device recall · Class II · Flower Orthopedics Corporation
Key facts
| Recall number (Z-number) | Z-0113-2022 |
|---|---|
| Recall event | 88669 |
| Product | Flower Drill Bit Kit 2.7mm- The Drill Bit Kit, 2.7mm (DBK 027) is intended to be used with solid 2.7mm screws and can be used with any the Flower Small and Medium Implant Set Flower Ankle Plating Set , Flower Rear Foot/Calcaneus Plating Set or Flower Upper Extremity Plating Set and uses the medium… |
| Product code | HTW |
| Recalling firm | Flower Orthopedics Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 16, 2023 |
| 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