Device recall
Z-2786-2020: Calcaneus Plate, Extensile, Medium, Right, Catalog Number CPF 202 - Product…
FDA device recall · Class II · Flower Orthopedics Corporation
Key facts
| Recall number (Z-number) | Z-2786-2020 |
|---|---|
| Recall event | 86023 |
| Product | Calcaneus Plate, Extensile, Medium, Right, Catalog Number CPF 202 - Product Usage: intended to be used for internal fixation of fractures and reconstruction of bones of the rearfoot, including the calcaneus. |
| Product code | HRS |
| Recalling firm | Flower Orthopedics Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 8, 2020 |
| 510(k) numbers | K133930 |
| FEI number | 3009996260 |
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