Device recall
Z-3084-2026: 5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6
FDA device recall · Class II · Fresenius Medical Care Renal Therapies Group, LLC
Key facts
| Recall number (Z-number) | Z-3084-2026 |
|---|---|
| Recall event | 99556 |
| Product | 5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6 |
| Product code | KOC |
| Recalling firm | Fresenius Medical Care Renal Therapies Group, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K243505 |
| FEI number | 3001451489 |
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