Device recall
Z-2428-2020: Ally Bone Screw - Product Usage:Bone Screws are indicated for use in bone…
FDA device recall · Class II · PROVIDENCE MEDICAL TECHNOLOGIES
Key facts
| Recall number (Z-number) | Z-2428-2020 |
|---|---|
| Recall event | 85111 |
| Product | Ally Bone Screw - Product Usage:Bone Screws are indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation appropriate for the size of the device. Screws are intended for single use only. L Providence Medical Technology, Inc. 3875 Hopyard… |
| Product code | HWC |
| Recalling firm | PROVIDENCE MEDICAL TECHNOLOGIES |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 27, 2022 |
| 510(k) numbers | K121713 |
| FEI number | 3009394448 |
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