Device recall
Z-2784-2016: Adaptor for Small Battery Drive and Small Battery Drive II. Product Usage: The…
FDA device recall · Class I · The Anspach Effort, Inc.
Key facts
| Recall number (Z-number) | Z-2784-2016 |
|---|---|
| Recall event | 74835 |
| Product | Adaptor for Small Battery Drive and Small Battery Drive II. Product Usage: The Light Adaptor for Small Battery Drive (SBD) /Small Battery Drive II (SBD II) is designed for use in traumatology and orthopedic surgery of the skeleton, i.e. drilling, reaming or cutting bone. The Adaptors (05.001.024 and… |
| Product code | HWE |
| Recalling firm | The Anspach Effort, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 9, 2018 |
| 510(k) numbers | K043310 |
| FEI number | 1045834 |
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