Device recall
Z-0647-2017: Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The…
FDA device recall · Class I · Centurion Medical Products Corporation
Key facts
| Recall number (Z-number) | Z-0647-2017 |
|---|---|
| Recall event | 75536 |
| Product | Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The Multi-Med catheter is indicated for use in patients requiring administration of solutions, blood sampling, and central venous pressure monitoring. |
| Product code | FOZ |
| Recalling firm | Centurion Medical Products Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 20, 2017 |
| 510(k) numbers | K955839 |
| FEI number | 3008403546 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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