Device recall
Z-1029-04: Circle C Dual Lumen Acute Hemodialysis/Apheresis Catheter Surgical Tray…
FDA device recall · Class II · Horizon Medical Products Inc
Key facts
| Recall number (Z-number) | Z-1029-04 |
|---|---|
| Recall event | 29253 |
| Product | Circle C Dual Lumen Acute Hemodialysis/Apheresis Catheter Surgical Tray, DLC-600TEC, 12 Fr. x 15.2cm, Sterile, Manufactured by: Horizon Medical Products, Inc., One Horizon Way, P.O. Box 627, Manchester, GA 31816, 1-800-472-5221. The product is a clear rigid plastic surgical tray containing… |
| Product code | KOC |
| Recalling firm | Horizon Medical Products Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 12, 2005 |
| 510(k) numbers | K941851 |
| FEI number | 3017892510 |
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