Device recall
Z-0089-06: Medrad Overhead Counterpoise System II. Support Arm. Mount Injector Head…
FDA device recall · Class II · Medrad Inc
Key facts
| Recall number (Z-number) | Z-0089-06 |
|---|---|
| Recall event | 33816 |
| Product | Medrad Overhead Counterpoise System II. Support Arm. Mount Injector Head. Catalog numbers 3010544, 3010545, 3010546, 3010547, 3010548, 3010549, 3010550, 3010551, 3010552, and 3010553. |
| Product code | JAK |
| Recalling firm | Medrad Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 29, 2007 |
| 510(k) numbers | K944983 |
| FEI number | 2520313 |
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