Device recall
Z-0550-05: Brand Name of Device: EmpowerCT/EmpowerCTA Injector System Ceiling Column…
FDA device recall · Class II · E-Z-EM, Inc
Key facts
| Recall number (Z-number) | Z-0550-05 |
|---|---|
| Recall event | 31007 |
| Product | Brand Name of Device: EmpowerCT/EmpowerCTA Injector System Ceiling Column Accessory; Common/Usual Name: CT Injector System Ceiling Column Accessory, Catalog Number 9886L. Ceiling Column Accessory: The CT and CTA Injector Systems employs an Articulating Arm that mounts to the Ceiling Column… |
| Product code | JAK |
| Recalling firm | E-Z-EM, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 24, 2007 |
| 510(k) numbers | K011160, K031571 |
| FEI number | 2411512 |
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