Device recall
Z-0859-2009: CombiSet True Flow Series, Hemodialysis Blood Tubing with Priming Set and…
FDA device recall · Class II · Fresenius Medical Care North America
Key facts
| Recall number (Z-number) | Z-0859-2009 |
|---|---|
| Recall event | 50491 |
| Product | CombiSet True Flow Series, Hemodialysis Blood Tubing with Priming Set and Transducer Protectors, with Access Flow Reversing Connector (Twister) Product Code: 03-2994-6 24 sets / case CombiSet Bloodlines Including split-septum injection site, viral-retentive transducer protectors, & priming set &… |
| Product code | KOC |
| Recalling firm | Fresenius Medical Care North America |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 24, 2009 |
| 510(k) numbers | K022536 |
| 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