Device recall
Z-0702-2019: Presource Kit Total Joint Pack containing a double-wrapped basin component…
FDA device recall · Class II · Cardinal Health Inc.
Key facts
| Recall number (Z-number) | Z-0702-2019 |
|---|---|
| Recall event | 81756 |
| Product | Presource Kit Total Joint Pack containing a double-wrapped basin component. Product Usage: This kit is used on patients undergoing joint replacement knee or hip. |
| Product code | LRO |
| Recalling firm | Cardinal Health Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 4, 2019 |
| FEI number | 3007329020 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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