Device recall
Z-1919-2025: Kendall SCD Blended Comfort Sleeves Knee Length Small - For use with Kendall SCD…
FDA device recall · Class II · Cardinal Health 200, LLC
Key facts
| Recall number (Z-number) | Z-1919-2025 |
|---|---|
| Recall event | 96849 |
| Product | Kendall SCD Blended Comfort Sleeves Knee Length Small - For use with Kendall SCD SmartFlow SKU 84021B Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow Controller |
| Product code | JOW |
| Recalling firm | Cardinal Health 200, LLC |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K230028 |
| FEI number | 3001236905 |
At a glance
- 1–9 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