Device recall
Z-0256-05: LifePort, Dual Lumen Profile Plastic Dual Port with Poly Urethane Catheter Kit…
FDA device recall · Class II · Horizon Medical Products Inc
Key facts
| Recall number (Z-number) | Z-0256-05 |
|---|---|
| Recall event | 30048 |
| Product | LifePort, Dual Lumen Profile Plastic Dual Port with Poly Urethane Catheter Kit, Product Code/REF: LPS 7255, Manufactured by: Horizon Medical Products, Inc., One Horizon Way, P.O. Box 627, Manchester, GA 31816.The devices are placed in a molded PVC tray. The tray is sealed with a Tyvek lid. The inner… |
| Product code | LJT |
| Recalling firm | Horizon Medical Products Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 1, 2005 |
| 510(k) numbers | K953529 |
| FEI number | 3017892510 |
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