Device recall
Z-1852-2008: HydraGlide XL Heparin Coated Silicone Thoracic Catheters, Increased number of…
FDA device recall · Class II · Atrium Medical Corporation
Key facts
| Recall number (Z-number) | Z-1852-2008 |
|---|---|
| Recall event | 48124 |
| Product | HydraGlide XL Heparin Coated Silicone Thoracic Catheters, Increased number of eyelets, Increased Length by 6", Atrium Code # 14720, Size 20, # Eyelets 15, 10 per case |
| Product code | GBZ |
| Recalling firm | Atrium Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 20, 2009 |
| FEI number | 3011175548 |
At a glance
- None Linked 510(k)s
- 10–99 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