Device recall
Z-0295-2019: Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product Usage: The…
FDA device recall · Class II · Arthrex, Inc.
Key facts
| Recall number (Z-number) | Z-0295-2019 |
|---|---|
| Recall event | 81106 |
| Product | Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product Usage: The battery housing is used to house the battery that powers the AR-400 DrillSaw Sports 400 device. |
| Product code | HAB |
| Recalling firm | Arthrex, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1220246 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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